PORTABLE PERSONAL HAND SANITIZER DISPENSER
A dispensing apparatus includes a cartridge containing a liquid. The cartridge has an opening covered by a sealing element. A piercing element in the apparatus pierces the sealing element, and as liquid is dispensed from the cartridge, the seal deforms in response to negative pressure to allow air to enter the cartridge. The cartridge may additionally or alternatively have an aperture covered by a gas permeable but liquid impermeable membrane. The apparatus may include a valve proximate to the outlet thereof. The valve may comprise an obstructing element biased against a valve seat by a resilient member. Fluid pressure from a metering mechanism in the apparatus may displace the obstructing element from the valve seat to thereby permit liquid to flow through the outlet.
This application is a continuation in part of U.S. patent application Ser. No. 18/159809 filed on 26 Jan. 2023, which is a continuation of International Patent Application No. PCT/CA 2021/051052 filed on 27 Jul. 2021, which claims priority to, and the benefit of, U.S. patent application Ser. No. 63/057,060, filed 27 Jul. 2020. Each of the foregoing applications are incorporated by reference herein for all purposes.
TECHNICAL FIELDThere is provided a sanitizer dispenser. In particular, there is provided a portable personal hand sanitizer dispenser.
BACKGROUNDThere is a general desire to maintain hand hygiene to avoid transmission of germs and diseases. This is particularly relevant for front-line workers such as healthcare workers, members of fire departments, and members of the police. Individuals working in these positions often require clean hands, but may not always have access to running water and soap to wash their hands. The demanding nature of front-line work is such that rapid response to emergency situations is often required, and therefore convenient access to hand sanitizer is essential. For this reason, there remains a need for a method of sanitizing one's hands that is fast and effective, yet also convenient.
The foregoing examples of the related art and limitations related thereto are intended to be illustrative and not exclusive.
United States Patent Application Publication No. 2013/0068791 A1 to Pelfrey et al. discloses a portable dispenser providing a light source that is configured to illuminate a dispensing nozzle, indicia carried upon the dispenser housing, and the refill container when the dispenser is actuated to dispense material therefrom. As such, the dispenser conveniently identifies the intended region at which the material is to be dispensed, while providing a compelling and entertaining manner of operation.
United States Patent Application Publication No. 2003/0019536 A1 to Smith discloses a type of institutional or hospital network system of personal, portable hand cleaning agent dispensers and a method to record and report their specific usage by healthcare workers and patients of the institution or hospital through a dispenser control apparatus having a computer processor memory. In one form, each dispenser has an identifier unique to it and shared with no other dispenser. Each dispenser contains hand cleaning fluid agent in an amount sufficient to provide multiple shots of predetermined amount (or unit dose size) upon pressing a pad on the dispenser to dispense one shot per press. Each worker has an identifier unique to that worker. In one form, dispensers are refillable and are issued from and returned to a control station that refills the dispensers and for each of them, records into a computer, the dispenser by that dispenser's unique identifier, the worker by that worker's unique identifier, and the quantity of hand cleaning fluid used by said dispenser, and reports from the data collected by said computer, who used what dispenser, during what time frame, and how much hand cleaning fluid was used by said worker using said dispenser during said time frame. In other forms, the dispensers have replaceable throw-away, agent-containing cartridges of single or multiple storage compartments, the dispensers being refillable with new cartridges from control and release stations.
United States Patent Application Publication No. 2013/0299533 A1 to Gronewoller et al. discloses a holster for an electronic device that may have a pair of flexible hollow cushions that may hold the device in the holster. The cushions may be flexible enough to allow the device to be held in the holster both with and without a protective cover over the device. The cushions may have a hollow portion that collapses when compressed during insertion of the device. The cushion material may be a molded silicone that may have a nonslip surface finish. In some embodiments, the cushion may protrude through a bottom surface of the holster to provide a nonslip foot when the holster is used as a stand support for the device.
United States Patent Application Publication No. 2013/334248 A1 to Iseri et al. discloses a dispenser for hand sanitizer. A sanitizer dispenser may comprise a dispenser intake, a diaphragm pump comprising a diaphragm and a pump chamber, a dispenser outlet, a first one-way valve having an intake in fluid communication with the dispenser intake and an output in fluid communication with the pump chamber, a second one-way valve having an intake in fluid communication with the pump chamber and an outlet in fluid communication with the dispenser outlet, and a push plate comprising an outer surface and configured to press an outer surface of the diaphragm when the push plate is pressed.
United States Patent Application Publication No. 2010/0094581 to Cagle discloses a hand-held personal liquid dispenser including a pump and pump plunger that dispenses liquid from a reservoir inside the dispenser when depressed. The dispenser includes circuitry that detects and records each depression of the plunger, and a port for connection to an external computer to transfer data such as identifiers for the dispenser and its user, and time and date of dispenser usage. A tracking and reporting system is disclosed that allows for the collection of nationwide data for standards per setting and health care worker and the report of same.
SUMMARYThe following embodiments and aspects thereof are described and illustrated in conjunction with systems, tools and methods which are meant to be exemplary and illustrative, not limiting in scope. In various embodiments, one or more of the above-described problems have been reduced or eliminated, while other embodiments are directed to other improvements.
One aspect provides a wearable personal dispensing apparatus comprising: a housing; an attachment interface affixed to the housing and operable to affix the dispensing apparatus to an item of clothing; an outlet on the housing; a replaceable cartridge containing a fluid; an electrically-powered metering mechanism fluidly connected to the outlet; and an engagement interface on the housing, the engagement interface operable to control the metering mechanism to dispense a volume of the fluid from the outlet.
In some embodiments, the fluid is hand sanitizer.
The item of clothing could be a belt. The attachment interface could be a clip. In some embodiments, the clip is biased to a generally closed position by a bias mechanism. A detent may be provided to hold the clip in a generally open position against the force applied by the bias mechanism. In some embodiments, the dispensing apparatus can be stably supported in an upright position on a surface while the clip is being held in the generally open position by the detent.
In some embodiments, the attachment interface comprises one or more of: a hook and loop fastener; one or more magnets; and a MOLLE connector.
The engagement interface comprises a control operable by a person such as an engagement interface and/or button. In some embodiments, the control is recessed in the housing. In some embodiments, the engagement interface is centered from side to side on the housing.
The engagement interface is operable to control the metering mechanism to dispense the fluid. The metering mechanism may be configured to dispense a prescribed volume of fluid each time the engagement interface is operated.
The metering mechanism may be located below the cartridge. In some embodiments, the metering mechanism comprises a pump that is fluidly connected between the replaceable cartridge and the outlet. In some embodiments, the pump is electrically powered. A battery may supply electrical power to operate the dispensing apparatus. The battery may be rechargeable. In some embodiments, the battery is rechargeable via a USB recharging interface. In some embodiments, the battery is disposable. The battery could be, for example, an AA, AAA, D, or C type battery. Some embodiments include an indicator that indicates a level of charge remaining in the battery.
The replaceable cartridge could have a breakable seal that is punctured upon the cartridge being inserted into the dispensing apparatus. The seal could be puncturable by a spur that is fluidly connected to the outlet. In some embodiments, the tip of the spur is tapered. A gasket may surround the seal.
In some embodiments, the replaceable cartridge is disposable. In some embodiments, the replaceable cartridge is recyclable. Replaceable cartridges containing different types of fluid may be provided.
In some embodiments, the replaceable cartridge is accessible by way of a door formed in the housing. The door may be located on one side of the housing. The door may have a latch (e.g. a latch comprising a pair of magnets) to facilitate access to the replaceable cartridge.
The replaceable cartridge may span most (e.g. at least 80% or at least 85%) of the way side to side across the housing. The replaceable cartridge may be inserted sideways into the housing. A pull tab may be provided to assist with removal of the replaceable cartridge. The pull tab may contain instructions for operation of the dispensing apparatus.
In some embodiments, the replaceable cartridge is sized to hold 40 millimeters (mL) ±20 mL of fluid.
Some embodiments include a fluid level indicator that is operated when the remaining amount of the fluid in the replaceable cartridge has been reduced below a prescribed level. The fluid level indicator may, for example, comprise a light and/or an audible indicator. For example, a sound emitted by a speaker could signify that the fluid in the replaceable cartridge has reached a prescribed level.
In some embodiments, the cartridge is comprised of a semi-rigid or rigid material.
In some embodiments, the height of the housing is 150 millimeter (mm) or less or 120 mm or less or 100 mm or less.
In some embodiments, the width of the housing is 100 mm or less or 70 mm or less.
In some embodiments, the depth of the housing is 40 mm or less or 30 mm or less or 25 mm or less.
In some embodiments, the dispensing apparatus weighs in the range of 4 oz (ounces) to 6 oz.
In some embodiments, the housing comprises a grommet at the interface between the housing and the engagement interface, the housing and the attachment interface, the housing and the door, the housing and the outlet, and around the edges of the housing. In some embodiments, the housing is impact resistant. The housing may be configured to have rounded edges.
The housing may, for example, comprise plastic, metal, or leather. In some embodiments, the housing is dust resistant, preferably dust and moisture resistant. The housing may for example have an ingress protection rating of IP45 or IP67.
Another aspect of the invention provides a dispensing apparatus comprising: a housing, an outlet on the housing, an attachment interface on the housing, a fluid contained in a replaceable cartridge, an actuator fluidly connected to the outlet and the fluid, an engagement interface on the housing, and a means for dispensing the fluid by engaging with the engagement interface.
Another aspect provides a dispensing apparatus comprising: a housing; an outlet on the housing; a clip affixed to the housing, wherein the clip has a first end and a second end, wherein the clip has a hinge, wherein the hinge is sprung such that the second end of the clip is forced into contact with the housing, wherein a detent is affixed to the housing, wherein the detent is operable to hold the first end of the clip against the force of the hinge thereby holding the second end of the clip away from the housing; hand sanitizer contained in a cartridge that is replaceable, wherein the hand sanitizer is fluidly connected to the outlet on the housing, wherein the cartridge has a seal that can be punctured, wherein the dispensing apparatus has a spur that is configured to puncture the seal when the cartridge is inserted into the dispensing apparatus; a button on the housing operable to dispense a volume of the hand sanitizer upon engaging with the engagement interface, wherein an electric pump dispenses the volume of the hand sanitizer, and wherein the electric pump is powered by a rechargeable battery.
Another aspect provides a dispensing apparatus comprising: a housing having an outlet; a rigid or semi-rigid replaceable cartridge having an interior shaped to receive a liquid therewithin and an opening via which the interior is accessible; an elastomeric sealing element which couples to the cartridge and covers said opening; a piercing element that pierces through the elastomeric sealing element when the cartridge is inserted into the housing; and a metering mechanism fluidly connected to the piercing element and the outlet, the metering mechanism operable to draw the liquid from the cartridge so inserted into the housing, to the outlet, wherein operation of the metering mechanism to dispense the liquid generates a negative pressure within the cartridge, and wherein the elastomeric sealing element deforms in response to the negative pressure to allow air to enter the cartridge via the opening as the liquid is removed therefrom.
In some embodiments, the sealing element includes a generally tubular body coaxial with said opening and a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, with the central membrane being positioned within the interior of the cartridge.
In some embodiments, the sealing element includes a generally tubular body coaxial with said opening and a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element and wherein the central membrane has a thickness that is generally less than that of the tubular body and/or decreases from a periphery thereof towards a center thereof.
In some embodiments, the sealing element has a longitudinally-extending exterior which tapers in a direction extending an outer end portion towards an inner end portion thereof and/or wherein the sealing element is rotationally symmetric about a longitudinal axis thereof.
In some embodiments, the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the sealing element includes a first flange shaped to abut with an interior surface of the cartridge a second flange shaped to abut an exterior surface of the cartridge, the first and second flanges coupling to and extending radially outwards from the tubular body of the sealing element, with each said flange spanning a lateral extent greater than of said opening, and with the sealing element coupling to the cartridge at least in part via said first flange and the second flange.
In some embodiments, the sealing element has an inner end positionable within the interior of the cartridge and an outer end positionable outwards from the cartridge, wherein the first flange tapers in a direction extending from the outer to the inner end of the cartridge, wherein the second flange tapers in a direction extending from the inner to the outer end of the cartridge, wherein the flanges are spaced-apart a distance equal to or less than a wall thickness of the cartridge adjacent said opening, and/or wherein the central membrane of the sealing element aligns with the first flange of the sealing element.
In some embodiments, the sealing element has an inner end positionable within the interior of the cartridge, an outer end axially spaced from the inner end thereof and positionable outwards from the cartridge, an outer bore which extends from the outer towards the inner end of the cartridge and an inner bore which extends from the inner towards the outer end of the cartridge, wherein the sealing element includes a laterally-extending central membrane extending between the outer and inner bores thereof, and wherein the central member and/or inner bore are adjacent the inner end of the cartridge.
In some embodiments, the outer bore tapers in a direction extending from the outer end towards the inner end of the cartridge and/or wherein the inner bore tapers in a direction extending from the outer end towards the inner end of the cartridge, wherein the outer bore is generally or substantially frustoconical in lateral section and/or wherein the inner bore is generally or substantially frustoconical in lateral section.
In some embodiments, the sealing element includes an inner annular surface which extends about the outer bore thereof and wherein the sealing element includes an annular portion which couples to and extends radially inwards from the inner annular surface thereof, wherein the annular portion of the sealing element is adjacent the outer end of the sealing element, wherein the annular portion of the sealing element has an inner diameter which is less than an outer diameter of the piercing element, and/or wherein the annular portion of the sealing element is an isosceles trapezoid in lateral section.
In some embodiments, the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, and wherein the central membrane and/or piercing element are configured and/or sized so as to enable a sealing force of central membrane exerted on an outer surface of the piercing element to be overcome upon the pressure differential between atmospheric pressure and pressure within cartridge reaching and/or exceeding a set and/or predetermined threshold.
In some embodiments, the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the sealing element deforms to allow air to be drawn into the cartridge at least in part in the form of: the central membrane moving away and/or outwards from the piercing element; the central membrane moving radially outwards from an outer surface of the piercing element; an interior surface of the central membrane becoming outwardly concave and/or more outwardly concave; an exterior surface of the central membrane becoming outwardly convex and/or more outwardly convex; and/or the central membrane moving both longitudinally inwards and radially outwards relative to the piercing element.
In some embodiments, the apparatus includes a mounting assembly comprising: a mount affixed to the housing including a plurality of mount magnets and a backing plate including a plurality of backing plate magnets, wherein the backing plate is arrangeable relative to the mount so as to align each of the backing plate magnets with a respective one of the mount magnets to thereby magnetically couple the backing plate to the mount; and/or an elasticated band operatively connected to the housing and positionable on an arm of a user of the dispensing apparatus.
Another aspect provides a replaceable cartridge for a personal dispensing apparatus, the cartridge comprising: a rigid or semi-rigid hollow body having an interior within which a liquid is receivable, the body having spaced-apart first and second apertures each in fluid communication with the interior thereof; and a membrane coupled to the body so as to cover the first aperture, wherein the membrane inhibits passage of the liquid therethrough, and enables passage of gas therethrough to relieve negative pressure generated when the liquid is dispensed through the second aperture.
In some embodiments, the membrane is secured to the body via induction sealing; and/or an adhesive.
In some embodiments, the membrane is: a thin, microporous membrane, wherein the membrane is waterproof and breathable.
In some embodiments, the first aperture has a diameter generally or substantially equal to less than 1 mm; and/or wherein the membrane comprises expanded polytetrafluoroethylene.
Another aspect provides a personal dispensing apparatus comprising: a housing having an outlet; a metering mechanism for dispensing a fluid out of the outlet; and a valve positioned on a fluid path between the metering mechanism and the outlet, the valve including a obstructing element, a valve seat, a channel, and a resilient member positioned within the channel, wherein the resilient member biases the obstructing element into sealing engagement with the valve seat via a spring force, and wherein fluid pressure from the metering mechanism overcomes the spring force so as to dislodge the obstructing element from the valve seat and thereby permit the fluid to flow around the obstructing element and through the channel to the outlet on the housing.
In some embodiments, the valve has a valve inlet and a valve outlet, wherein the valve outlet is smaller than the valve inlet, wherein the valve in part functions as a nozzle and/or wherein the valve is shaped to jet the liquid outwards from the valve outlet thereof.
In some embodiments, the valve is positioned at the outlet of the housing, and wherein a longitudinal axis of the valve is positioned at a non-parallel angle relative to longitudinal and lateral axes of the housing.
In some embodiments, the valve includes one or more valve bodies which are continuously tubular from proximal to distal ends thereof so as to inhibit passage of fluid radially therethrough.
Another aspect provides a system for recording actuation data, the system comprising: a local device; and a personal dispensing apparatus including a dispensing mechanism to dispense fluid, a local memory, a physical port, and a processor, wherein the personal dispensing apparatus records via the processor an actuation record in the local memory in response to an actuation of the dispensing mechanism, and wherein the personal dispensing apparatus transmits via the processor the actuation record from the local memory to the local device via the physical port.
In addition to the exemplary aspects and embodiments described above, further aspects and embodiments will become apparent by reference to the drawings and by study of the following detailed descriptions.
Exemplary embodiments are illustrated in referenced figures of the drawings. It is intended that the embodiments and figures disclosed herein are to be considered illustrative rather than restrictive:
Throughout the following description, specific details are set forth in order to provide a more thorough understanding to persons skilled in the art. However, well known elements may not have been shown or described in detail to avoid unnecessarily obscuring the disclosure. Accordingly, the description and drawings are to be regarded in an illustrative, rather than a restrictive, sense.
Dispensing apparatus 20 includes housing 22, engagement interface 24, and outlet 26. Dispensing apparatus 20 is operable to release a fluid (e.g. hand sanitizer). Dispensing apparatus 20 includes an actuator 42 seen in
Engagement interface 24 may be hand-operated. For example, engagement interface 24 is depicted as a button 24B in
As best seen in
Housing 22 surrounds components internal to dispensing apparatus 20. Housing 22 may comprise a rigid material. For example, housing 22 may comprise: metal such as, but not limited to, aluminum or an aluminum alloy; or plastic such as, but not limited to polyethylene or polycarbonate. The rigid material(s) provide impact resistance for dispensing apparatus 20. Housing 22 may also comprise a semi-rigid material, such as but not limited to leather or fabric. Housing 22 may have rounded edges so as to avoid catching on other objects (such as clothing, car seats, etc.). In some embodiments, housing 22 has dust resistance, and preferably has dust and moisture resistance. In some embodiments, housing 22 has an IP45 rating for ingress protection. In some embodiments, housing 22 has an IP67 rating for ingress protection, which provides complete protection from ingress of dust, and ingress protection against water when submersed for 30 minutes at a depth of 1 meter.
Apparatus 20 is preferably compact to allow apparatus 20 to be comfortably worn by an individual. In some embodiments, the height (represented by dimension H in
Apparatus 20 is preferably thin. A ratio of depth to height (D:H) is preferably 1:4 or less. A ratio of depth to width to height (D:W) is preferably 1:3 or less.
As described in more detail below, fluid to be dispensed by dispensing apparatus 20 is provided in cartridges 32. This facilitates rapidly refilling of dispensing apparatus 20 upon depletion of a given cartridge. The cartridges may be rigid or semi-rigid cartridges.
As seen in
Cartridges 32 may have a thin flat construction with a sufficient volume of fluid while allowing dispensing apparatus 20 to be thin. In some embodiments, cartridges 32 may be a rectangular prism in shape.
Housing 22 of dispensing apparatus 20 contains attachment interface 28. Attachment interface 28 is configured such that dispensing apparatus 20 can be worn by an individual. Attachment interface 28 is configured to attach dispensing apparatus 20 to an individual's clothing.
Attachment interface 28 may be configured such that the entire attachment interface attaches to an individual's clothing, a preferred construction of which is shown in
In some embodiments, attachment interface 28 comprises two separable parts. One of the parts may be attached (removably or non-removably) to an individual's clothing; the other part may be attached to housing 22. The two parts have a coupling that enables the two parts to be detachably affixed to one another. In some embodiments, attachment interface 28 comprises a hook and loop fastener such as Velcro™. One component of the hook and loop fastener is affixed to housing 22, and the other component of the hook and loop fastener is affixed to a desired object such as a piece of clothing. In some embodiments, one component of the hook and loop fastener is affixed to the dashboard of a motor vehicle, and the other component of the hook and loop fastener mechanism is affixed to housing 22. In other embodiments, one component of the hook and loop fastener mechanism is affixed to a piece of furniture, and the other component of the hook and loop fastener mechanism is affixed to housing 22. In some embodiments, attachment interface 28 comprises a magnet affixed to housing 22. The magnet may then be used to hold dispensing apparatus 20 to any ferrous metal material. In some embodiments, attachment interface 28 comprises a pair of magnets, with one of the magnets affixed to an individual's clothing, and the other magnet affixed to housing 22.
Referring to
When detent 29 is engaged with first end 27A of clip 27, attachment interface 28 is in an open position. Maintaining attachment interface 28 in the open position is advantageous if one wishes to affix attachment interface 28 to an item of clothing, as it reduces the dexterity needed to affix attachment interface 28 to an item of clothing while also depressing first end 27A of clip 27 against the force of hinge 27C.
In some embodiments, clip 27 is configured to allow a user to stand dispensing apparatus 20 on a surface. When clip 27 is in the open position, second end 27B of clip 27 and the bottom of housing 22 form a base on which dispensing apparatus 20 can be rested.
In some embodiments, to revert attachment interface 28 from the open position to the closed position, a user depresses first end 29A of detent 29. Depressing first end 29A of detent 29 bends detent 29 about detent stem 29C. Bending detent 29 about detent stem 29C releases first end 27A of clip 27 from second end 29B of detent 29. Once first end 27A of clip 27 is released, hinge 27C causes attachment interface 28 to close by biasing second end 27B of clip 27 back into contact with housing 22.
As seen in
Attachment interface 28 as described herein enables a user to affix dispensing apparatus 20 to an item of clothing. Given that dispensing apparatus 20 can be worn by an individual, the colour of housing 22 on dispensing apparatus 20 may be customized. In some embodiments, the colour, design and/or texture of housing 22 may be customized or customizable to match a uniform design. For example, housing 22 could have a camouflage design if being used by a member of a military. In some embodiments, housing 22 is customized to display a logo. For example, housing 22 may bear a logo or a coat of arms of an organization.
Dispensing apparatus 20 may include a latch operable to hold door 30 in a closed position.
In some embodiments, the latch comprises a pair of magnets 30B which hold door 30 closed when door 30 is in a closed position (shown in
Other embodiments may use different approaches to allow access to the interior of dispensing apparatus 20. For example, in some embodiments, door 30 is configured to have a set of pins on one side, with a clip on the opposite side, with receptacles for the pins and clip on housing 22. In some embodiments, door 30 is omitted to enable easy access to remove and replace cartridge 32.
Cartridge 32 is held inside cavity 35 in housing 22. Cartridge 32 holds fluid to be dispensed. Cartridge 32 is replaceable. Upon the fluid within the cartridge 32 being generally or substantially dispensed, a user can open door 30 to remove cartridge 32, and place a new cartridge 32 in cavity 35 of dispensing apparatus 20. Cartridge 32 preferably has a rigid or semi-rigid construction. Cartridge 32 may comprise a rigid or semi-rigid material.
In some embodiments, a pull tab is provided to assist with the removal of cartridge 32 from dispensing apparatus 20. For example, as shown in
In some embodiments, pull tab 33 contains graphical and/or textual instructions for use of dispensing apparatus 20. In some embodiments, the pull tab is affixed to chassis 37, wrapping around cartridge 32 when cartridge 32 is inserted into dispensing apparatus 20. Pulling on the pull tab in this embodiment partially removes cartridge 32 from dispensing apparatus 20, enabling easier removal of cartridge 32 from dispensing apparatus 20.
Cartridge 32 contains a fluid. In particular, cartridge 32 is intended to contain a fluid that can be used as hand sanitizer. The hand sanitizer may, for example, comprise an alcohol-based hand sanitizer or any other hand sanitizer.
Cartridge 32 is depicted as having a substantially rectangular flattened shape. In some embodiments, cartridge 32 has a different shape, for example (but not limited to) a cylinder, a cube, or an ellipsoid.
Spur 36 is tubular such that it forms a through passage through which liquid can flow. Tip 36A of spur 36 is configured to provide a pointed edge that can pierce seal 34. An end portion of spur 36 near tip 36A may be tapered in diameter. The taper of spur 36 may interface with a corresponding surface inside seal 34 to improve the fluid-tight seal between spur 36 and cartridge 32.
Seal 34 is made from a material that keeps fluid contained within cartridge 32 while cartridge 32 is not in use and that can be pierced by spur 36 when cartridge 32 is inserted within dispensing apparatus 20. By way of non limiting examples, seal 34 may comprise a polymer, an elastomer, a thin sheet of aluminum, an aluminum plastic laminate, and/or a sheet of plastic-coated paper.
Gasket 34A may be provided on the perimeter of seal 34. Gasket 34A, when present, may help to improve sealing between cartridge 32 and spur 36. When cartridge 32 is moved in direction 32B and spur 36 pierces seal 34, gasket 34A encircles spur perimeter 36B, thereby creating a fluid-tight seal. Gasket 34A is preferably made of a deformable material such as rubber to further improve the fluid-tight seal between cartridge 32 and spur 36.
In some embodiments, cartridge 32 includes a vent which allows air to enter cartridge 32 as fluid is removed from cartridge 32. In some embodiments, small amounts of air are allowed to enter cartridge 32 through the interface between seal 34 and spur 36 or through seal 34 as fluid is withdrawn from cartridge 32. In some embodiments, portions of one or more walls of cartridge 32 are thin such that upon pressure being reduced within cartridge 32, a part of the wall of cartridge 32 is deformed. In some embodiments, dispensing apparatus 20 includes a stylet or needle or the like that punctures cartridge 32 to provide a vent when cartridge 32 is inserted into dispensing apparatus 20. For example, the stylet or the like may be provided on the inner wall of chamber 31 or on door 30 so that an air hole is pricked in cartridge 32 upon cartridge 32 being inserted into dispensing apparatus 20 or upon door 30 being closed.
When cartridge 32 is moved in direction 32B and spur 36 pierces seal 34, spur 36 will be fluidly connected to the liquid inside of cartridge 32. The liquid inside of cartridge 32 can then flow from cartridge 32 through the tubular through passage formed by spur 36.
There are at least two advantages associated with cartridge 32 being replaceable. One advantage is that a replaceable cartridge enables rapid replenishment of the fluid carried by dispensing apparatus 20. A user of dispensing apparatus 20 can carry spare cartridges 32 with them to enable continued and extended use of dispensing apparatus 20. The cartridges may be sturdy, rigid, or semi-rigid cartridges that can be safely stored in a pocket, glove compartment or the like. A second advantage associated with cartridge 32 being replaceable is that it enables a user to change the fluid being dispensed from dispensing apparatus 20 (for example, changing from hand sanitizer to ointment), as the apparatus will dispense whatever fluid is contained within cartridge 32.
In some embodiments, cartridge 32 is refillable. In some embodiments, cartridge 32 is recyclable. In some embodiments, cartridge 32 is disposable. In some embodiments, cartridge 32 is both recyclable and disposable.
In some embodiments, dispensing apparatus 20 includes an indicator which indicates when a cartridge 32 needs replacing and/or the amount of fluid remaining in cartridge 32. The indicator may, for example, be visual and/or audible. Some embodiments provide an indicator light on housing 22 that illuminates upon the amount of fluid remaining in the cartridge reaching a prescribed level. Some embodiments include an electroacoustic transducer that emits a noise when the amount of fluid remaining in the cartridge 32 reaches a prescribed level. The electroacoustic transducer may, for example, comprise a speaker, a buzzer or the like. In some embodiments, the visual indicator comprises a display (e.g. an OLED display or an LCD display) located on housing 22 that provides a readout indicative of an amount of fluid remaining in cartridge 32.
Given the small form-factor of dispensing apparatus 20, it is not possible for dispensing apparatus 20 to contain large amounts of fluid for dispensing without becoming unwieldy when worn by an individual due to the weight of dispensing apparatus 20. For this reason, cartridge 32 may have a capacity of, for example, 40 mL of fluid. Because of the relatively small volume of fluid held by cartridge 32, cartridge 32 is replaceable. This enables continued and extended use of small and light weight dispensing apparatus 20. In some embodiments, dispensing apparatus 20 weighs less than 6 oz or 7 oz. For example, dispensing apparatus 20 may weigh in the range of 4 to 6 oz.
The metering mechanism is actuated to dispense a quantity of fluid from outlet 26 in response to engagement interface 24 being operated (e.g. by a user pressing or touching engagement interface 24 with their hand). When the metering mechanism is actuated, actuator 42 dispenses a prescribed volume of fluid from cartridge 32 to outlet 26.
In the example embodiment of
Some embodiments include an indicator that indicates the level of power remaining in power source 40. The indicator may, for example, be visual and/or audible. For example, in some embodiments, the power level indicator comprises an indicator light. The indicator light may, for example, be an LED (light emitting diode). In some embodiments, the power level indicator is located on or near recharging interface 41. In some embodiments, the power level indicator is located on housing 22.
Dispensing apparatus 20 includes a grommet 39 seen in
In some embodiments, actuator 42 is customizable to dispense a particular volume of fluid or dosage. For example, actuator 42 may be configured to dispense fluid in 1 mL or 2 mL increments upon operation of engagement interface 24. In some embodiments, actuator 42 is configured to dispense fluid in increments ranging between 0.5 mL to 20 mL. In some embodiments, actuator 42 is configured dispense or meter out a dosage generally or substantially in conformity with World Health Organization (WHO) and/or Centers for Disease Control and Prevention (CDC) mandated dosage protocols.
Upon engaging with engagement interface 24, an electronic circuit controls delivery of power to actuator 42 through wires 44 and 46. The electronic circuit may be configured to supply power to actuator 42 for a prescribed period and/or a prescribed number of pulses, thereby dispensing a desired quantity of the fluid at outlet 26. The length of the prescribed period and/or the number of pulses may be customizable to adjust how much fluid actuator 42 dispenses each time it is triggered by operation of engagement interface 24. The longer the prescribed period and/or the more pulses, the more fluid will be dispensed. Upon the expiration of the prescribed period, power to the actuator is stopped, thereby stopping the fluid from being dispensed.
In some embodiments, actuator 42 is a pump of a type that delivers a set amount of fluid per cycle. In such embodiments actuator 42 may be operated for one or more cycles (depending on the desired amount of fluid to be released) each time engagement interface 24 is operated. In some embodiments, actuator 42 comprises a pump having an adjustable cycle volume and the amount of fluid to be released is adjustable by adjusting the cycle volume of the pump.
As described herein, dispensing apparatus 20 may be used by front line workers to protect themselves and to protect persons with whom they may come into contact. The apparatus may be implemented in situations that require convenient and immediate access to hand sanitizer. By facilitating rapid access to hand sanitizer, the apparatus can improve the safety of the front line workers themselves, and the individuals they are serving. For example, a police officer may use dispensing apparatus 20 to maintain access to hand sanitizer throughout the day. The police officer could attach dispensing apparatus 20 to their belt. The police officer would likely be wearing a belt containing bulky equipment, and as such, they would first lift second end 27B of clip 27 such that first end 27A of clip 27 is held in place by detent 29. The police officer could then place clip 27 over their belt, and press first end 29A of detent 29 to release first end 27A of clip 27. At this point, dispensing apparatus 20 would be affixed to the police officer's belt by clip 27. Then, as required, the police officer can engage with engagement interface 24 to release hand sanitizer from dispensing apparatus 20. Since engagement interface 24 is placed on a portion of housing 22 that is recessed, accidental engagements with engagement interface 24 are avoided. If dispensing apparatus 20 runs out of hand sanitizer, then the police officer can quickly open door 30 on the side of housing 22, remove cartridge 32, and insert a replacement cartridge 32.
At the end of the day, the police officer may remove dispensing apparatus 20 from their belt. If they find themselves completing paperwork at a desk, they can stand dispensing apparatus 20 on their desk by lifting second end 27B of clip 27 such that first end 27A of clip 27 is held in place by detent 29. Second end 27B of clip 27 and the bottom of housing 22 then form a base on which dispensing apparatus 20 can stand for easy access.
As liquid is drawn from cartridge 32.1 by the metering mechanism, a negative pressure may be generated in cartridge 32.1. As shown in
In the example embodiment shown in
In some embodiments, sealing element 110 comprises a laterally-extending or central membrane 116. Central membrane 116 extends across an interior 115I of tubular body 115. Central membrane 116 is piercable by piercing element 120.
In some embodiments, sealing element 110 has a radially outwardly extending tapered surface 114 seen in
In some embodiments, sealing element 110 is rotationally symmetric about longitudinal axis 110A.
In the example embodiment shown in
In some embodiments, second flange 113B extends radially outwards from tubular body 115 to a greater extent than first flange 113A.
In some embodiments, sealing element 110 comprises inner end portion 110I and outer end portion 110O. Inner end 110I may be positionable within an interior 32.1I of cartridge 32.1 (shown in
In some embodiments, sealing element 110 has inner bore 118I and outer bore 118O. Outer bore 118O may extend from outside of cartridge 32.1 towards interior 32.1I of cartridge 32.1. Inner bore 118I may extend from interior 32.1I of cartridge 32.1 towards outside of cartridge 32.1. Inner bore 118I may be adjacent interior 32.1I of cartridge 32.1.
In some embodiments, outer bore 118O tapers in a direction extending outside of cartridge 32.1 towards interior 32.1I of cartridge 32.1 (i.e., in the direction represented by arrow 119A in
In some embodiments, outer bore 118O is generally or substantially frustoconical in lateral section and/or inner bore 118I is generally or substantially frustoconical in lateral section.
In some embodiments, sealing element 110 includes inner annular surface 118OS which extends about outer bore 118O. In this example, sealing element 110 includes an annular portion 118A positioned within interior 115I of tubular body 115. Annular portion 118A of sealing element 110 couples to and extends radially inwards from inner annular surface 118OS in this example. Annular portion 118A may be near or adjacent outer end 110O of sealing element 110. Annular portion 118A may have a diameter DA less than an outer diameter DO of sealing element 110. In some embodiments, annular portion 118A may comprise an isosceles trapezoid in lateral section.
In some embodiments, sealing element 110 comprises a polymer, in this example an elastomer, in this non-limiting case ethylene propylene diene monomer rubber; however, the latter is not strictly required and the sealing element may be made of materials in other examples. In some embodiments, sealing element 110 has a Shore A hardness of less than or equal to 60. In some embodiments, sealing element 110 is made of a material that is resistant to ethyl alcohol. In some embodiments, sealing element 110 is black. In some embodiments, a volume of sealing element 110 is approximately 0.12 cc (cubic centimeters).
As the metering mechanism removes liquid from cartridge 32.1, the gas pressure within interior 32.1I of cartridge 32.1 may reduce below the ambient gas pressure outside of cartridge 32.1. This pressure differential (which may be referred to as a negative pressure) is undesirable as it may cause deformation of cartridge 32.1. The negative pressure may additionally or alternatively place increased strain on the metering mechanism, potentially impairing the ability of the metering mechanism to draw liquid from cartridge 32.1.
When there is a negative pressure in cartridge 32.1, sealing element 110 deforms to allow air to be drawn into cartridge 32.1, thereby increasing the pressure within cartridge 32.1.
Without wishing to be bound by theory, the inventor posits that when there is a negative pressure in cartridge 32.1, a higher pressure is exerted on an exterior surface 116E of central membrane 116 than on interior surface 116I of central membrane 116. In embodiments where membrane 116 is flexible and/or elastomeric, this pressure differential causes the central membrane 116 to deform inwardly toward interior 32.1I of cartridge 32.1, as shown in
Central membrane 116 of sealing element 110 and/or piercing element 120 are thus configured and/or sized so as to enable the sealing force of central membrane 116 exerted on outer surface 120OS of piercing element 120 to be overcome upon the pressure differential between atmospheric pressure and pressure within cartridge 32.1 reaching and/or exceeding a set and/or predetermined threshold. Sealing element 110 deforms to allow air to be drawn into cartridge 32.1 at least in part in the form of central membrane 116 moving away and/or outwards from piercing element 120, in this non-limiting example moving radially outwards from outer surface of piercing element 120. Sealing element 110 deforms to allow air to be drawn into cartridge 32.1 at least in part in the form of interior surface 116I of central membrane 116 becoming outwardly concave and/or more outwardly concave. Sealing element 110 deforms to allow air to be drawn into cartridge 32.1 at least in part in the form of exterior surface 116E of central membrane 116 becoming outwardly convex and/or more outwardly convex in one non-limiting embodiment. Sealing element 110 deforms to allow air to be drawn into cartridge 32.1 at least in part in the form of central membrane 116 moving both longitudinally inwards and radially outwards relative to piercing element 120 according to another non-limiting example.
In some embodiments and referring back to
Membrane 131 may couple to cartridge 32.1 using various methods. By way of non-limiting example, membrane 131 may couple to cartridge 32.1 by way of induction sealing. In some embodiments, membrane 131 is coupled to cartridge 32.1 by way of an adhesive.
In some embodiments, aperture 130 is less than 1 mm in diameter.
Although the example embodiment shown in
Valve 140 has an inlet 142A and an outlet 142B. In some embodiments, inlet 142A is fluidly connected to piercing element 120 or spur 36. In some embodiments, outlet 142B couples to outlet 26.1 of dispensing apparatus 20.1 or outlet 26 of dispensing apparatus 20. In some embodiments, valve 140 is selectively removable and/or replaceable. In this non-limiting example, an exterior of valve 140 comprises one or more ribs 140R. In embodiments where valve 140 is press fit into housing 22.1 of apparatus 20.1, ribs 140R facilitate a secure press fit installation of valve 140 thereto. As seen in
In some embodiments, outlet 142B has a diameter 142BD that is equal to or less than half of a diameter 142AD of the valve inlet in one non-limiting embodiment, equal to or less than ⅖th of that of the valve inlet in another non-limiting embodiment and equal to or less than ⅓rd of that of the valve inlet in a further non-limiting embodiment. The valve outlet diameter is less than 0.35 mm in one non-limiting example, less than 0.30 mm in another non-limiting example, and less than 0.21 mm in a further non-limiting example.
As shown in the cross-sectional view of
A liquid pressure may be exerted on valve 140 at inlet 142A (e.g., via a metering mechanism coupled to cartridge 32.1). Upon the liquid pressure at inlet 142A reaching a level sufficient to overcome the spring force of biasing member 147, obstructing element 144 is dislodged from valve seat 146, as shown in
When the liquid pressure at inlet 142A drops below a level sufficient to overcome the spring force of biasing member 147, obstructing element 144 is biased into sealing engagement with valve seat 146 by the spring force of biasing member 147. The spring force of biasing member 147 is configured and/or selected to inhibit inadvertent dripping of fluid outwards from outlet 142B. In some embodiments, the cracking pressure of valve 140 (i.e., the liquid pressure at which obstructing element is dislodged from valve seat 146) is less than 14 kPa (kilopascal).
Valve outlet 142B is shaped to jet liquid outwards therefrom, in this example by being smaller than valve inlet 142A in this example, so as to promote said jetting of liquid outwards therefrom. In some embodiments, obstructing element 144 is spherical in shape, and valve seat 146 includes a radially inwardly extending shoulder 146S.
In some embodiments, valve 140 includes a first, proximal or inlet valve body 140I which extends from inlet 142A towards outlet 142B thereof. Inlet valve body 140I is tubular and has a first or proximal end 140I-1 adjacent inlet 142A and a second or distal end 140I-2 spaced-apart longitudinally from the proximal end 140I-1 thereof. Ribs 140R extend from proximal end 140I-1 towards distal end 140I-2 of inlet valve body 140I in this example. Inlet valve body 140I includes a tubular portion 140I-T which extends continuously from distal end 140I-2 to ribs 140R so as to inhibit passage of fluid therethrough. Inlet valve body 140I has a first or inner bore 140II extending from proximal end 140I-1/inlet 142A towards distal end 140I-2/outlet 142B thereof. Inlet valve body 140I has a second or outer bore 140IO and a shoulder 146S forming valve seat 146 and which extends radially between inner 140II and outer bores 140IO thereof. Inlet valve body 140I may thus be said to comprise and/or function as a seat for obstructing element 144.
In some embodiments, valve 140 includes a second, distal or outlet valve body 140O which extends from outlet 142B towards inlet 142A and which is shaped to substantially extend within outer bore 140IO of inlet valve body 140I thereof in this non-limiting example. Outlet valve body 140O is tubular and includes a first, distal, enlarged or flanged end portion 140O-1 adjacent outlet 142B and shaped to abut distal end 140I-2 of inlet valve body 140I. Outlet valve body 140O includes a second, proximal end portion 140O-2 longitudinally spaced-apart from the flanged end portion 140O-1 thereof in this example. Proximal end portion 140O-2 of outlet body extends at a non-perpendicular angle relative to longitudinal axis 143 and/or may be said to comprise or be formed via a diagonal or miter cut. Outlet valve body 140O is insertable within outer bore 140IO of inlet valve body 140I via proximal end portion 140I-2 thereof.
Outlet valve body 140O has a first or outer bore 140OO extending from outlet 142B towards inlet 142A, a second or inner bore 140OI shaped to receive biasing member 147 therein, and a shoulder or biasing member seat 140OS extending radially between the inner bore 140OI and outer bores 140OO thereof and upon which an outer end 147O of biasing member 147 abuts. In this non-limiting example, outlet valve body 140O selectively couples to inlet valve body 140I (e.g. via threadable coupling or otherwise) so as to enable selective access to obstructing element 144 and/or biasing member 147 for replacement thereof and/or to selectively control and/or adjust the extent to which biasing member 147 biases against obstructing element 144 and thus selectively adjust/control said cracking pressure of valve 140. Outer bore 140OO of outlet valve body of valve 140 corresponds to outlet 142B of valve and is smaller than inner bore 140OI of outlet valve body 140O of valve 140, as well as smaller than inner 140II and outer bores 140IO of inlet valve body 140I. Outlet valve body 140O and/or valve 140 as a whole may be referred to and/or comprise a nozzle.
As shown in the exploded view in
Armband 160 comprises band 161 that is positionable on an arm of a user. In some embodiments, band 161 is elasticated.
In the example embodiment shown in
In some embodiments, armband 160 is adjustable. By way of example, a circumference of band 161 may be adjusted by an adjustment mechanism comprising buckle 163 and fastener 162. In the example embodiment shown in
Referring to
Referring back to
The method next includes detecting via processor 182-1 an actuation of a dispensing mechanism by user 181 (e.g., upon actuation of actuator 42.1 to release fluid from apparatus 20.1), with the processor transitioning from the low power sleep state thereof in step 172A to an active state. The method at step 172B may thus be said to comprise configuring processor 182-1 to transition from the low power sleep state to said active state upon detecting one or more actuations of the actuator. In addition or alternatively, the method at step 172B may thus be said to comprise configuring processor 182-1 to wake-up upon receiving one or more signals indicative of actuation of the actuator and/or upon receiving one or more actuation signals. Step 172B may further including detecting via processor 182-1 one or more features about the actuation. In the example embodiment shown in
In some embodiments, the method includes only recording via processor 182-1 actuation record 172C-1 if a configurable and/or predetermined and/or minimum threshold volume of fluid is dispensed. The method may include monitoring via processor 182-1 the dispensing mechanism of apparatus 20.1 to assess whether a dispensing mechanism operation cycle corresponding to the configurable volume has completed. The method may thus include, for example, configuring processor 182-1 to refrain from recording or logging an actuation record 172C-1 in step 172 where the dispensing mechanism operation cycle was interrupted and/or determined to be interrupted. By way of example, in embodiments where the fluid being dispensed by apparatus 20.1 is hand sanitizer, a hygienically effective volume of hand sanitizer may be 2 mL (in this example, the configurable volume of fluid). If it is known that actuator 42.1 must operate for at least 1 second to dispense 2 mL of hand sanitizer, then the dispensing mechanism operation cycle is 1 second long. Consequently, in some embodiments, processor 182-1 may only record actuation record 172C-1 upon detecting that actuator 42.1 has run for at least 1 second. In some embodiments, processor 182-1 may only record actuation record 172C-1 upon detecting that actuator 42.1 has run for at least 1.5 seconds. Thus, step 172 may include refraining from recording or logging the actuator record: i) upon determining via processor 182-1 that an actuation time is less than a predetermined minimum threshold and/or time and/or 1 or 1.5 seconds; and/or upon determining via processor 182-1 that a volume of fluid dispensed 172B-2 for a given actuation of the actuator is less than a predetermined minimum threshold and/or volume and/or 2 mL.
The method includes at step 172C, adding via processor 182-1 actuation record 172C-1 to actuation record set 172C-2 stored in local memory 182-2 of apparatus 20.1.
Upon completion of step 172C, the method includes placing processor 182-1 in a low power sleep state once more and/or configuring processor 182-1 to enter a low power sleep state anew. Steps 172A to 172C may be repeated a plurality of times (e.g., over the course of a shift of a healthcare worker) to provide a plurality of actuation records 172-1 in actuation record set 172C-2.
Referring back to
Upon establishing the physical coupling, processor 182-1 of apparatus 20.1 may detect the connection and transmit the actuation record set 172C-2 from local memory 182-2, through hardwired connection 182-4, to local device 183, where it may be stored in local memory 183-2. In some embodiments, device 183 may be a Raspberry Pi™, or another suitable computing device.
In some embodiments, local device 183 is coupleable to a plurality of apparatus 20.1 via separate hardwired connections 182-4 at once. By way of example, local device may be couplable via hardwired connections 182-4 to between 1 and 50 apparatus 20.1 at once.
Because dispensing apparatus 20.1 lacks wireless connectivity, internal clock 182-3 cannot continuously synchronize with an authoritative external time source during use. The inability to continuously synchronize may lead to gradual deviation (also known as “clock drift”) during use of apparatus 20.1, causing actuation times associated with actuation records 172C-1 to become inaccurate.
Method 176 begins at step 176A comprising receiving via processor 183-1 of local device 183 dispenser time 176A-1. Dispenser time 176A-1 corresponds to a current time as reported by internal clock 182-3 of apparatus 20.1.
Step 176B comprises determining a time offset 176B-2 between dispenser time 176A-1 and a concurrently obtained authoritative time 176B-1 from authoritative time source 183-3. In some embodiments, authoritative time source 183-3 comprises a network-synchronized time source. Time offset 176B-2 may be calculated by taking the difference between authoritative time 176B-1 and dispenser time 176A-1. By way of example, if the difference between authoritative time 176B-1 and dispenser time 176A-1 is positive, this indicates that the time reported by internal clock 182-3 of apparatus 20.1 is behind authoritative time 176B-1. A positive time offset 176B-2 would then need to be applied to actuation record set 172C-2 to adjust actuation times 172B-1 of each actuation record 172C-1. By way of further example, if the difference between authoritative time 176B-1 and dispenser time 176A-1 is negative, this indicates that the time reported by internal clock 182-3 is ahead of authoritative time 176B-1. A negative time offset 176B-2 would then need to be applied to actuation record set 172C-2 to adjust actuation times 172B-1 of each actuation record 172C-1.
Step 176C comprises applying time offset 176B-2 to actuation times 172B-1 in each actuation record 172C-1 in actuation record set 172C-2 to obtain certified actuation record set 176D-1. Certified actuation record set 176D-1 may represent a more accurate record of dispensing events associated with apparatus 20.1.
In some embodiments, the method may include analyzing via processor 183.1 of local device 183 actuation record set 172C-2 to identify large temporal gaps between actuations, which may indicate periods of device inactivity or power loss. The method may include configuring processor 183-1 to omit actuation records 172C-1 which comprise and/or are determined to comprise temporal gaps which exceed a predetermined threshold, as they may be erroneously created entries (e.g., due to power fluctuations or the like).
In some embodiments, the method may include transmitting certified actuation record set 176D-1 from local device 183 to centralized server 184 for analysis by organization 185.
By way of example, a healthcare worker, such as a nurse, may use apparatus 20.1 throughout their shift, generating an actuation record set 172C-2 stored in local memory 182-2. Over the course of the day, the internal clock 182-3 of apparatus 20.1 may drift and become, for example, 45 seconds slower relative to the hospital's network time or network protocol time (in this example, authoritative time source 183-3). At the end of the shift, the nurse physically couples apparatus 20.1 to local device 183, such as a docking station or hub at a hospital, to transmit actuation record set 172C-2.
Upon establishing the connection, local device 183 compares current time 176A-1 from the internal clock 182-3 with authoritative time 176B-1 from authoritative time source 183-3 and determines a time offset 176B-2 of-45 seconds. The local device's processor 183-1 then applies this −45 second correction to every preliminary timestamp in actuation record set 172C-2 received from apparatus 20.1. An actuation that was locally recorded at 14:30:00 on apparatus 20.1 is thus verified as having instead occurred at 14:29:15. This generates a certified actuation record set 176D-1, which provides a more accurate record to prove to organization 185 (e.g., a hospital) that, for example, a nurse sanitized their hands using apparatus 20.1 after finishing their break and before returning to care for patients. Such records may be subsequently correlated to specific actions taken by the person for quality control and/or regulatory compliance purposes or the like.
As mentioned above, in some embodiments actuator 42 is configured dispense or meter out a dosage generally or substantially in conformity with WHO and/or CDC mandated dosage protocols. The exact CDC required dosage is dispensed thereby creating an actual loggable health regulated protocol of sanitation including time and date and serial number of device and dispersing the required health protocols, Apparatus 20.1 as herein described may thus at the point of contact provide proof that a user or clinician is adhering to point of contact mandates set forth in various health acts or standards, such as, in one non-limiting example, the CSA Z317.12:25 Canadian standard entitled “Cleaning and disinfecting of health care facilities”. Under the CSA Z317.12:25 update, the “Point of Care” mandate requires that the dispensing volume be auditable and the apparatuses as herein described may provide such functionality. Apparatus 20.1 as herein described provides an actuator or pump which outputs liquid at a pressure of 8 to 14 PSI in one non-limiting embodiment and 10 PSI in a further non-limiting embodiment and this, together with check valve 140, may result in fluid being dispensed by the apparatus with a variance of between 1.2 ml and 1.5 ml in one non-limiting embodiment. The latter may be much tighter than traditional pump-action units of the known prior art and may comprise a standard operating delivery amount. Apparatus 20.1 as herein described may thus provide the data needed for “Validated Clean hands” mandates. In addition, apparatuses 20/20.1 as herein described may further be manufactured in compliance with and/or taking into account International Organization for Standardization (ISO) 10993-10.
Interpretation of TermsUnless the context clearly requires otherwise, throughout the description and the claims:
-
- “comprise”, “comprising”, and the like are to be construed in an inclusive sense, as opposed to an exclusive or exhaustive sense; that is to say, in the sense of “including, but not limited to”;
- “connected”, “coupled”, or any variant thereof, means any connection or coupling, either direct or indirect, between two or more elements; the coupling or connection between the elements can be physical, logical, or a combination thereof;
- “herein”, “above”, “below”, and words of similar import, when used to describe this specification, shall refer to this specification as a whole, and not to any particular portions of this specification;
- “or”, in reference to a list of two or more items, covers all of the following interpretations of the word: any of the items in the list, all of the items in the list, and any combination of the items in the list;
- the singular forms “a”, “an”, and “the” also include the meaning of any appropriate plural forms.
Words that indicate directions such as “vertical”, “transverse”, “horizontal”, “upward”, “downward”, “forward”, “backward”, “inward”, “outward”, “left”, “right”, “front”, “back”, “top”, “bottom”, “below”, “above”, “under”, and the like, used in this description and any accompanying claims (where present), depend on the specific orientation of the apparatus described and illustrated. The subject matter described herein may assume various alternative orientations. Accordingly, these directional terms are not strictly defined and should not be interpreted narrowly.
While processes or blocks are presented in a given order, alternative examples may perform routines having steps, or employ systems having blocks, in a different order, and some processes or blocks may be deleted, moved, added, subdivided, combined, and/or modified to provide alternatives or subcombinations. Each of these processes or blocks may be implemented in a variety of different ways. Also, while processes or blocks are at times shown as being performed in series, these processes or blocks may instead be performed in parallel, or may be performed at different times.
In addition, while elements are at times shown as being performed sequentially, they may instead be performed simultaneously or in different sequences. It is therefore intended that the following claims are interpreted to include all such variations as are within their intended scope.
Where a component (e.g. a housing, an attachment interface, an actuator etc.) is referred to above, unless otherwise indicated, reference to that component (including a reference to a “means”) should be interpreted as including as equivalents of that component any component which performs the function of the described component (i.e., that is functionally equivalent), including components which are not structurally equivalent to the disclosed structure which performs the function in the illustrated exemplary embodiments of the invention.
Specific examples of systems, methods and apparatus have been described herein for purposes of illustration. These are only examples. The technology provided herein can be applied to systems other than the example systems described above. Many alterations, modifications, additions, omissions, and permutations are possible within the practice of this invention. This invention includes variations on described embodiments that would be apparent to the skilled addressee, including variations obtained by: replacing features, elements and/or acts with equivalent features, elements and/or acts; mixing and matching of features, elements and/or acts from different embodiments; combining features, elements and/or acts from embodiments as described herein with features, elements and/or acts of other technology; and/or omitting combining features, elements and/or acts from described embodiments.
Various features are described herein as being present in “some embodiments”. Such features are not mandatory and may not be present in all embodiments. Embodiments of the invention may include zero, any one or any combination of two or more of such features. This is limited only to the extent that certain ones of such features are incompatible with other ones of such features in the sense that it would be impossible for a person of ordinary skill in the art to construct a practical embodiment that combines such incompatible features. Consequently, the description that “some embodiments” possess feature A and “some embodiments” possess feature B should be interpreted as an express indication that the inventors also contemplate embodiments which combine features A and B (unless the description states otherwise or features A and B are fundamentally incompatible).
Additional DescriptionExamples of wearable personal dispensing apparatuses have been described. The following clauses are offered as further description.
(1) A wearable personal dispensing apparatus comprising: a housing; an attachment interface affixed to the housing and operable to affix the dispensing apparatus to an item of clothing; an outlet on the housing; a replaceable cartridge containing a fluid; an electrically-powered metering mechanism fluidly connected to the outlet; and an engagement interface on the housing, the engagement interface operable to control the metering mechanism to dispense a volume of the fluid from the outlet.
(2) The wearable personal dispensing apparatus of any clause herein, wherein the fluid is hand sanitizer.
(3) The wearable personal dispensing apparatus of any clause herein, wherein the item of clothing is a belt and wherein the attachment interface is configured to couple the housing to the belt.
(4) The wearable personal dispensing apparatus of any clause herein, wherein the attachment interface on the housing is a clip.
(5) The wearable personal dispensing apparatus of any clause herein, including a bias mechanism operable to bias the clip to a generally closed position.
(6) The wearable personal dispensing apparatus of any clause herein, comprising a detent that is operable to hold the clip in a generally open position against the force applied by the bias mechanism.
(7) The wearable personal dispensing apparatus of any clause herein, wherein the dispensing apparatus can be placed on a surface while the clip is held in a generally open position by the detent.
(8) The wearable personal dispensing apparatus of any clause herein, wherein the attachment interface is a hook and loop fastener.
(9) The wearable personal dispensing apparatus of any clause herein, wherein the attachment interface comprises a pair of magnets.
(10) The wearable personal dispensing apparatus of any clause herein, wherein the attachment interface is a MOLLE connector.
(11) The wearable personal dispensing apparatus of any clause herein, wherein the engagement interface is centered on the housing.
(12) The wearable personal dispensing apparatus of any clause herein, wherein the engagement interface is a button.
(13) The wearable personal dispensing apparatus of any clause herein, wherein the button is recessed in the housing.
(14) The wearable personal dispensing apparatus of any clause herein, wherein the button is operable to control the metering mechanism to dispense the fluid.
(15) The wearable personal dispensing apparatus of any clause herein, wherein the metering mechanism dispenses a prescribed volume of fluid.
(16) The wearable personal dispensing apparatus of any clause herein, wherein the metering mechanism is a pump that is fluidly connected to the replaceable cartridge and the outlet.
(17) The wearable personal dispensing apparatus of any clause herein, wherein the metering mechanism is located below the replaceable cartridge.
(18) The wearable personal dispensing apparatus of any clause herein, wherein the pump is electrically powered.
(19) The wearable personal dispensing apparatus of any clause herein, wherein the pump is electrically powered by a battery.
(20) The wearable personal dispensing apparatus of any clause herein, wherein the battery is rechargeable.
(21) The wearable personal dispensing apparatus of any clause herein, wherein the battery is rechargeable via a USB recharging interface.
(22) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes an indicator to indicate the level of charge remaining in the battery.
(23) The wearable personal dispensing apparatus of any clause herein, wherein the battery is disposable.
(24) The wearable personal dispensing apparatus of any clause herein, wherein the pump is electrically powered by one or more AA batteries, one more AAA batteries, one or more D batteries, and/or one or more C batteries.
(25) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge includes a breakable seal that punctures upon being inserted into the dispensing apparatus.
(26) The wearable personal dispensing apparatus of any clause herein, wherein the breakable seal is puncturable by a spur that is fluidly connected to the outlet.
(27) The wearable personal dispensing apparatus of any clause herein, wherein the tip of the spur is tapered.
(28) The wearable personal dispensing apparatus of any clause herein, wherein a gasket surrounds the breakable seal.
(29) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge is disposable.
(30) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge is recyclable.
(31) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge is replaceable with another replaceable cartridge containing a different fluid.
(32) The wearable personal dispensing apparatus of any clause herein, including a door formed in and/or pivotably coupled to the housing.
(33) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge is accessible via the door.
(34) The wearable personal dispensing apparatus of any clause herein, wherein the door is formed on a side of the housing.
(35) The wearable personal dispensing apparatus of any clause herein, wherein the door includes a latch comprised of a pair of magnets.
(36) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge spans almost all the entire way across the housing.
(37) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge is inserted sideways into the housing.
(38) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge includes a pull tab.
(39) The wearable personal dispensing apparatus of any clause herein, wherein the pull tab contains an instruction manual.
(40) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge holds 40 ml_ of fluid.
(41) The wearable personal dispensing apparatus of any clause herein, including an indicator light which illuminates upon the remaining amount of the fluid in the replaceable cartridge reaching a prescribed level.
(42) The wearable personal dispensing apparatus of any clause herein, including a speaker via which a sound is emitted upon the amount of the fluid in the replaceable cartridge reaching a prescribed level.
(43) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge is semi-rigid or rigid.
(44) The wearable personal dispensing apparatus of any clause herein, wherein the height of the housing is less than 150 mm.
(45) The wearable personal dispensing apparatus of any clause herein, wherein the height of the housing is less than 120 mm.
(46) The wearable personal dispensing apparatus of any clause herein, wherein the height of the housing is less than 100 mm.
(47) The wearable personal dispensing apparatus of any clause herein, wherein the width of the housing is less than 100 mm.
(48) The wearable personal dispensing apparatus of any clause herein, wherein the width of the housing is less than 80 mm.
(49) The wearable personal dispensing apparatus of any clause herein, wherein the width of the housing is less than 70 mm.
(50) The wearable personal dispensing apparatus of any clause herein, wherein the depth of the housing is less than 40 mm.
(51) The wearable personal dispensing apparatus of any clause herein, wherein the depth of the housing is less than 30 mm.
(52) The wearable personal dispensing apparatus of any clause herein, wherein the depth of the housing is less than 25 mm.
(53) The wearable personal dispensing apparatus of any clause herein, wherein the housing comprises any one of, or combination of the following: plastic, metal, and leather.
(54) The wearable personal dispensing apparatus of any clause herein, wherein the housing comprises a grommet at the interface between the housing and the engagement interface, the housing and the attachment interface, the housing and the door, and around the edges of the housing.
(55) The wearable personal dispensing apparatus of any clause herein, wherein the personal dispensing apparatus has an ingress protection rating of IP45.
(56) The wearable personal dispensing apparatus of any clause herein, wherein the personal dispensing apparatus has an ingress protection rating of IP67.
(57) The wearable personal dispensing apparatus of any clause herein, wherein the housing is impact resistant.
(58) The wearable personal dispensing apparatus of any clause herein, wherein the housing has rounded edges.
(59) The wearable personal dispensing apparatus of any clause herein, wherein the wearable personal dispensing apparatus weighs between 4 and 6 oz (ounces).
(60) The wearable personal dispensing apparatus of any clause herein, wherein the housing has a front and a bottom, and wherein the outlet is angled relative to the front and the bottom of the housing.
(61) The wearable personal dispensing apparatus of any clause herein, wherein the outlet is angled at a non-perpendicular angle relative to the front and the bottom of the housing.
(62) The wearable personal dispensing apparatus of any clause herein, wherein the outlet is spaced upwards from the bottom of the housing.
(63) The wearable personal dispensing apparatus of any clause herein, wherein the outlet is positioned to direct fluid laterally outwards at least in part.
(64) The wearable personal dispensing apparatus of any clause herein, wherein the outlet is positioned to direct fluid both downwards at least in part and laterally outwards at least in part.
(65) The wearable personal dispensing apparatus of any clause herein, wherein the cartridge includes a vent which allows air to enter the cartridge as fluid is removed therefrom.
(66) The wearable personal dispensing apparatus of any clause herein, wherein at least some air is allowed to enter the cartridge through the interface between the seal and the spur or through the seal, as fluid is withdrawn from the cartridge.
(67) The wearable personal dispensing apparatus of any clause herein, wherein portions of one or more walls of the cartridge are thin such that upon pressure being reduced within the cartridge, a part of the wall of the cartridge is deformed.
(68) The wearable personal dispensing apparatus of any clause herein, including a stylet or needle that punctures the cartridge to provide said vent when the cartridge is inserted into the apparatus.
(69) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes a chamber within which the cartridge is received and wherein the stylet or needle is positioned on an inner wall of the chamber such that an air hole is formed in the cartridge upon the cartridge being inserted into the apparatus.
(70) The wearable personal dispensing apparatus of any clause herein, wherein the engagement interface is placed on a portion of the housing that is recessed.
(71) The wearable personal dispensing apparatus of any clause herein, wherein the engagement interface is position on and/or within a portion of the housing that is recessed to inhibit inadvertent actuation thereof.
(72) The wearable personal dispensing apparatus of any clause herein, wherein the stylet or needle is positioned on the door such that an air hole is formed in the cartridge upon the door being closed thereafter.
(73) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes a recessed portion which encloses the button at least in part.
(74) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes a recessed portion with a side wall which enclosed the button at least in part.
(75) The wearable personal dispensing apparatus of any clause herein, wherein the button is inwardly spaced from said side wall of the recessed portion of the housing.
(76) The wearable personal dispensing apparatus of any clause herein, wherein the side wall of the recessed portion of the housing is arcuate shaped and faces towards the front of the housing.
(77) The wearable personal dispensing apparatus of any clause herein, wherein the side wall has a first radius of curvature, and wherein the button has a second radius of curvature which is less than said first radius of curvature.
(78) The wearable personal dispensing apparatus of any clause herein, wherein the housing has a top and a rear, wherein the engagement interface is adjacent to and downwardly spaced from the top of the housing, and wherein the engagement interface is outwardly spaced from the rear of the housing.
(79) The wearable personal dispensing apparatus of any clause herein, wherein the engagement interface is inwardly positioned relative to a periphery of the housing.
(80) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes an outwardly extending protrusion adjacent to, at least partially enclosing and being shaped to inhibit inadvertent actuation of the engagement interface.
(81) The wearable personal dispensing apparatus of any clause herein, including a tape or ribbon configured to enable removable of the cartridge from the housing.
(82) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes an upper portion to which the engagement interface mounts and whose front, rear and sides each upwardly taper.
(83) The wearable personal dispensing apparatus of any clause herein, wherein the housing includes an upper portion which is an isosceles trapezoid in shape in front, rear and side profile.
(84) The wearable personal dispensing apparatus of any clause herein, wherein the replaceable cartridge has a substantially rectangular flattened shape.
(85) A wearable personal dispensing apparatus comprising: a housing; an outlet on the housing; an attachment interface on the housing operable to affix the dispensing apparatus to an item of clothing; a fluid contained in a replaceable cartridge; an actuator fluidly connected to the outlet and the fluid; an engagement interface on the housing; and a means for dispensing the fluid in response to engagement of the engagement interface.
(86) A wearable personal dispensing apparatus comprising: a housing; an outlet on the housing; a clip hingedly affixed to the housing by a hinge wherein the clip has a first end and a second end and the hinge is sprung such that the second end of the clip is biased toward being into contact with the housing; a detent affixed to the housing, the detent being operable to hold the first end of the clip against the force of the hinge thereby holding the second end of the clip away from the housing; hand sanitizer contained in a cartridge that is replaceable, wherein the hand sanitizer is fluidly connected to the outlet on the housing, the cartridge comprising a seal that can be punctured; a spur that is configured to puncture the seal when the cartridge is inserted into the dispensing apparatus; a control on the housing operable to trigger dispensing of a volume of the hand sanitizer by an electric pump powered by a rechargeable battery.
(87) A dispensing apparatus comprising: a housing having an outlet; a rigid or semi-rigid replaceable cartridge having an interior shaped to receive a liquid therewithin and an opening via which the interior is accessible; an elastomeric sealing element which couples to the cartridge and covers said opening; a piercing element that pierces through the elastomeric sealing element when the cartridge is inserted into the housing; and a metering mechanism fluidly connected to the piercing element and the outlet, the metering mechanism operable to draw the liquid from the cartridge so inserted into the housing, to the outlet, wherein operation of the metering mechanism to dispense the liquid generates a negative pressure within the cartridge, and wherein the elastomeric sealing element deforms in response to the negative pressure to allow air to enter the cartridge via the opening as the liquid is removed therefrom.
(88) The dispensing apparatus of any clause herein, wherein the sealing element includes a generally tubular body coaxial with said opening and a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, with the central membrane being positioned within the interior of the cartridge.
(89) The dispensing apparatus of any clause herein, wherein the sealing element includes a generally tubular body coaxial with said opening and a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element and wherein the central membrane has a thickness that is generally less than that of the tubular body and/or decreases from a periphery thereof towards a center thereof.
(90) The dispensing apparatus of any clause herein wherein the sealing element has a longitudinally-extending exterior which tapers in a direction extending an outer end portion towards an inner end portion thereof and/or wherein the sealing element is rotationally symmetric about a longitudinal axis thereof.
(91) The dispensing apparatus of any clause herein, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the sealing element includes a first flange shaped to abut with an interior surface of the cartridge a second flange shaped to abut an exterior surface of the cartridge, the first and second flanges coupling to and extending radially outwards from the tubular body of the sealing element, with each said flange spanning a lateral extent greater than of said opening, and with the sealing element coupling to the cartridge at least in part via said first flange and the second flange.
(92) The dispensing apparatus of any clause herein wherein the sealing element has an inner end positionable within the interior of the cartridge and an outer end positionable outwards from the cartridge, wherein the first flange tapers in a direction extending from the outer to the inner end of the cartridge, wherein the second flange tapers in a direction extending from the inner to the outer end of the cartridge, wherein the flanges are spaced-apart a distance equal to or less than a wall thickness of the cartridge adjacent said opening, and/or wherein the central membrane of the sealing element aligns with the first flange of the sealing element.
(93) The dispensing apparatus of any clause herein, wherein the sealing element has an inner end positionable within the interior of the cartridge, an outer end axially spaced from the inner end thereof and positionable outwards from the cartridge, an outer bore which extends from the outer towards the inner end of the cartridge and an inner bore which extends from the inner towards the outer end of the cartridge, wherein the sealing element includes a laterally-extending central membrane extending between the outer and inner bores thereof, and wherein the central member and/or inner bore are adjacent the inner end of the cartridge.
(94) The dispensing apparatus of any clause herein, wherein the outer bore tapers in a direction extending from the outer end towards the inner end of the cartridge and/or wherein the inner bore tapers in a direction extending from the outer end towards the inner end of the cartridge, wherein the outer bore is generally or substantially frustoconical in lateral section and/or wherein the inner bore is generally or substantially frustoconical in lateral section.
(95) The dispensing apparatus of any clause herein, wherein the sealing element includes an inner annular surface which extends about the outer bore thereof and wherein the sealing element includes an annular portion which couples to and extends radially inwards from the inner annular surface thereof, wherein the annular portion of the sealing element is adjacent the outer end of the sealing element, wherein the annular portion of the sealing element has an inner diameter which is less than an outer diameter of the piercing element, and/or wherein the annular portion of the sealing element is an isosceles trapezoid in lateral section.
(96) The dispensing apparatus of any clause herein, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, and wherein the central membrane and/or piercing element are configured and/or sized so as to enable a sealing force of central membrane exerted on an outer surface of the piercing element to be overcome upon the pressure differential between atmospheric pressure and pressure within cartridge reaching and/or exceeding a set and/or predetermined threshold.
(97) The dispensing apparatus of any clause herein, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the sealing element deforms to allow air to be drawn into the cartridge at least in part in the form of: the central membrane moving away and/or outwards from the piercing element; the central membrane moving radially outwards from an outer surface of the piercing element; an interior surface of
the central membrane becoming outwardly concave and/or more outwardly
concave; an exterior surface of the central membrane becoming outwardly convex and/or more outwardly convex; and/or the central membrane moving both longitudinally inwards and radially outwards relative to the piercing element.
(98) The dispensing apparatus of any clause herein, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the membrane so positioned flares outwards in a direction extending from an inner end portion towards an outer end portion of the sealing element, wherein the membrane is biased by the piercing element so as to enclose a
first space or passageway which is annular and which tapers in a direction extending from a periphery towards a center thereof, and wherein said deformation creates a temporary second space or passageway which is annular, wherein the second space or passageway is near or adjacent the center of the membrane and is in fluid communication with the first space or passageway.
(99) The dispensing apparatus of any clause herein including a mounting assembly comprising: a mount affixed to the housing including a plurality of mount magnets and a backing plate including a plurality of backing plate magnets, wherein the backing plate is arrangeable relative to the mount so as to align each of the backing plate magnets with a respective one of the mount magnets to thereby magnetically couple the backing plate to the mount; and/or an elasticated band operatively connected to the housing and positionable on an arm of a user of the dispensing apparatus.
(100) A replaceable cartridge for a personal dispensing apparatus, the cartridge comprising: a rigid or semi-rigid hollow body having an interior within which a liquid is receivable, the body having spaced-apart first and second apertures each in fluid communication with the interior thereof; and a membrane coupled to the body so as to cover the first aperture, wherein the membrane inhibits passage of the liquid therethrough, and enables passage of gas therethrough to relieve negative pressure generated when the liquid is dispensed through the second aperture.
(101) The replaceable cartridge of any clause herein wherein the membrane is secured to the body via induction sealing; and/or an adhesive.
(102) The replaceable cartridge of any clause herein, wherein the membrane is: a thin, microporous membrane, wherein the membrane is waterproof and breathable.
(103) The replaceable cartridge of any clause herein wherein the first aperture has a diameter generally or substantially equal to less than 1 mm (millimeter); and/or wherein the membrane comprises expanded polytetrafluoroethylene.
(104) A personal dispensing apparatus comprising: a housing having an outlet; a metering mechanism for dispensing a fluid out of the outlet; and a valve positioned on a fluid path between the metering mechanism and the outlet, the valve including a obstructing element, a valve seat, a channel, and a resilient member positioned within the channel, wherein the resilient member biases the obstructing element into sealing engagement with the valve seat via a spring force, and wherein fluid pressure from the metering mechanism overcomes the spring force so as to dislodge the obstructing element from the valve seat and thereby permit the fluid to flow around the obstructing element and through the channel to the outlet on the housing.
(105) The personal dispensing apparatus of any clause herein wherein the valve is a check valve.
(106) The personal dispensing apparatus of any clause herein wherein the valve has a valve inlet and a valve outlet, wherein the valve outlet is smaller than the valve inlet, wherein the valve in part functions as a nozzle and/or wherein the valve is shaped to jet the liquid outwards from the valve outlet thereof.
(107) The personal dispensing apparatus of any clause herein, wherein the spring force of the biasing member is configured and/or selected to inhibit inadvertent dripping of the fluid outwards from the valve outlet.
(108) The personal dispensing apparatus of any clause herein wherein the valve is positioned at the outlet of the housing.
(109) The personal dispensing apparatus of any clause herein wherein a longitudinal axis of the valve is positioned at a non-parallel angle relative to longitudinal and lateral axes of the housing.
(110) The personal dispensing apparatus of any clause herein wherein the valve (and/or the valve outlet thereof) comprises a last point of contact of the fluid.
(111) The personal dispensing apparatus of any clause herein, wherein the valve is shaped to press fit couple to the housing thereof.
(112) The personal dispensing apparatus of any clause herein, wherein the valve includes ribs via which the valve is press fit coupled to the housing.
(113) The personal dispensing apparatus of any clause herein, including a mount via which the valve selectively couples to and is removable from the housing.
(114) The personal dispensing apparatus of any clause herein, wherein the mount substantially encloses the valve and inhibits access and/or damage thereto.
(115) The personal dispensing apparatus of any clause herein, wherein the mount extends along a longitudinal axis which is non-parallel angle relative to a longitudinal axis and a lateral axis of the housing.
(116) The personal dispensing apparatus of any clause herein, wherein the mount is shaped to position a longitudinal axis of the valve at a non-parallel angle relative to the longitudinal and lateral axes of the housing.
(117) The personal dispensing apparatus of any clause herein, wherein the mount has an outwardly facing or outer face with an aperture extending through and an inner peripheral portion extending about and defining the aperture thereof, and wherein the longitudinal axis of the valve is coaxial with the longitudinal axis, face and/or aperture of the mount.
(118) The personal dispensing apparatus of any clause herein, wherein the outlet the valve is adjacent and in fluid communication with said aperture of the mount.
(119) The personal dispensing apparatus of any clause herein, wherein the mount (and/or outer face and/or aperture thereof) is shaped to extend about the valve outlet so as to form a space and/or an annular space therebetween.
(120) The personal dispensing apparatus of any clause herein, wherein the inner peripheral portion of the outer face of the mount is radially outwardly spaced from the valve outlet a distance selected to: inhibit inadvertent dispersal of liquid within and/or inwardly through the annular space; inhibit capillary action; inhibit a suck back action; inhibit inadvertent drippage of fluid; inhibit inadvertent dislodgement of the valve relative to mount; promote enclosure of and/or protection of the valve (and/or outlet thereof); and/or inhibit inadvertent, contaminated and/or outside contact with the valve (and/or outlet thereof). f
(121) The personal dispensing apparatus of any clause herein, wherein the inner peripheral portion of the outer face of the mount is radially outwardly spaced from the valve outlet a distance generally or substantially equal to or greater than 1 mm, generally or substantially equal to or less than 2 mm, and/or be generally or substantially equal to or less than 3 mm.
(122) The personal dispensing apparatus of any clause herein, wherein the valve has a valve inlet and a valve outlet, wherein the valve outlet has a diameter that is equal to or less than half of the diameter of the valve inlet.
(123) The personal dispensing apparatus of any clause herein, wherein the diameter of the valve outlet is equal to or less than ⅖th of the diameter of the valve inlet.
(124) The personal dispensing apparatus of any clause herein, wherein the diameter of the valve outlet is equal to or less than ⅓rd of the diameter of the valve inlet.
(125) The personal dispensing apparatus of any clause herein wherein the valve has a valve inlet and a valve outlet, wherein the valve outlet valve outlet diameter that is less than 0.35 mm, or less than 0.30 mm, or less than 0.21 mm.
(126) The personal dispensing apparatus of any clause herein, wherein the valve includes one or more valve bodies which are continuously tubular from proximal to distal ends thereof so as to inhibit passage of fluid radially therethrough.
(127) A method of recording actuation data, the method comprising: (a) dispensing a volume of fluid from an apparatus in response to actuation of a dispensing mechanism; (b) in response to the actuation of the dispensing mechanism, causing a suitably configured processor to record an engagement record in a local memory of the apparatus; and (c) transmitting the engagement record from the local memory to a separate external device via a physical port on the apparatus.
(128) The method of any clause herein, wherein the engagement record comprises a unique identifier associated with the apparatus and/or a timestamp associated with the actuation of the dispensing mechanism.
(129) The method of any clause herein, wherein the separate external device comprises a local gateway, and wherein the method further comprises transmitting the engagement record from the local gateway to a centralized database via a hardwired network connection.
(130) A system for recording actuation data, the system comprising a local device, and a personal dispensing apparatus having a dispensing mechanism to dispense fluid, a local memory, a physical port, and a processor configured to: record an actuation record in the local memory in response to an actuation of the dispensing mechanism; and transmit the actuation record from the local memory to the local device via the physical port.
(131) The system of any clause herein, wherein the processor is configured to record a plurality of actuation records in the local memory in response to a corresponding plurality of actuations of the dispensing mechanism to thereby obtain an actuation record set, and wherein the processor is further configured to transmit the actuation record set to the local device.
(132) The system of any clause herein, wherein the actuation record comprises a time of the actuation obtained from an onboard clock of the personal dispensing apparatus.
(133) The system of any clause herein, wherein the actuation record comprises a volume of fluid dispensed by the dispensing mechanism.
(134) The system of any clause herein, wherein the actuation record comprises a user identifier.
(135) The system of any clause herein, wherein the processor transitions from a low-power sleep state to an active state in response to the actuation to record the actuation record.
(136) The system of any clause herein, wherein the local device is further configured to analyze the actuation record by comparing the time of the actuation to an employee shift schedule.
(137) The system of any clause herein, wherein the time of actuation is a preliminary time of actuation, and wherein the local device is configured to: concurrently obtain an authoritative time from an authoritative time source, and a current time from the onboard clock of the dispensing apparatus; determine a temporal offset by comparing the current time from the onboard clock and the authoritative time from the authoritative time source; and apply the temporal offset to the preliminary time to generate a certified time of actuation.
(138) The system of any clause herein, wherein the personal dispensing apparatus lacks wireless transmission capability; wherein the personal dispensing apparatus is inhibited from transmitting data wirelessly; and/or wherein the personal dispensing apparatus is configured to only transmit data via a hardwired connection.
(139) The system of any clause herein, wherein the dispensing mechanism is operable to dispense a configurable volume of the fluid, and wherein the processor is further configured to record the actuation record only upon completion of a dispensing mechanism operation cycle corresponding to the configurable volume of fluid.
(140) The system of any clause herein, wherein the dispensing mechanism is operable to dispense a volume of the fluid, and wherein the personal dispensing apparatus records via the processor the actuation record only upon: completion of a dispensing mechanism operation cycle corresponding to the configurable, and/or predetermined and/or minimum threshold volume of fluid being dispensed; and/or an actuation time being equal to greater than a predetermined minimum threshold and/or time and/or 1 or 1.5 seconds.
(141) Apparatus including any new and inventive feature, combination of features, or sub-combination of features as described herein.
(142) Methods including any new and inventive steps, acts, combination of steps and/or acts or sub-combination of steps and/or acts as described herein.
Further DescriptionExamples of wearable personal dispensing apparatuses have been described and the following paragraphs are offered as yet a further description. The system/method as herein described may be referred to as a closed-loop hardwired ecosystem. The system/method comprises a physical handshake via a secure physical interface gate (e.g. via USB-C in one non-limiting example), with data only moving from dispensing apparatus 20 when physically docked. The system/method may comprise ethernet and/or be hardwired, thus providing a secure, shielded data transfer to the facility's server. The system/method as herein described is thus air-gapped. No Wi-Fi™, Bluetooth®, or any wireless protocols are used for data transfer from dispensing apparatus 20.
The technical “handshake” may thus comprise two physical stages: i) device-to-hub—the wearable device connects to a local hub such as via a multi-purpose USB-C port (handling both charging and the data “handshake”), and ii) hub-to-server-the hub (which may utilize a Raspberry Pi™ or similar microprocessor) then offloads that data to the facility's secure server via a Hardwired Ethernet Cable. The system/method as herein described may result in: superior security-immune to signal hacking or interception; zero interference, thus avoiding clutter of hospital Wi-Fi™ bands which may be critical for medical-grade EMC compliance; and a guaranteed audit trail-data cannot be “dropped”
due to a poor wireless signal, with the handshake only occurring when the physical connection is confirmed. The system/method as herein described may thus be referred to and/or comprise a deterministic event logger using deterministic tracking, as the data only exists because the physical engagement interface or button was pushed.
The microprocessor may use a “wake-on-interrupt” protocol—it stays in a state of near-zero power consumption until the mechanical depression of the dosing button closes a circuit. Dispensing apparatus 20 may include an onboard real-time clock (RTC), where at the millisecond the button is depressed, the microprocessor pulls the exact date and time and writes it to non-volatile memory. The onboard event logging may occur as follows: i) direct actuation trigger—the logging event is initiated via a mechanical-to-electronic interrupt (the dosing button), which ‘fully awakens’ the microprocessor from a deep-sleep state; ii) onboard temporal Attribution—dispensing apparatus 20 performs a local write of the Date and Time to a non-volatile ledger at the moment of actuation, iii) serial number marriage—dispensing apparatus 20 is tied to the user via a hard-coded serial number that is manually associated with the user's identity in the administrative database (manual marriage), eliminating the need for unreliable wireless ID tracking; iv) network independence-the microprocessor does not attempt to broadcast this data and, rather, stores the log locally until a physical handshake (e.g. USB-C) is established for data offload. The system/method as herein described may thus be referred to as an autonomous, hardwired event-logger which is self-authenticating and includes:
1. Deep-Sleep “Wake-on-Interrupt” Logic
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- The Hardware: The onboard microprocessor is “barely awake” (Deep Sleep) to maximize battery longevity. It is not a parasitic energy-harvesting system; it is a dedicated, event-triggered active node.
- The Trigger: The device fully awakens only when the mechanical dosing button is depressed. This mechanical-to-logic interrupt ensures power is only drawn during
the clinical event.
-
- Dispensing apparatus 20 utilizes a Wake-on-Interrupt Deep Sleep protocol. The microprocessor is electrically “dead” (consuming near-zero current) until the physical kinetic energy of the dosing cycle closes the circuit to “reanimate” the logic. This enables the 500-1,000 dose clinical duty cycle and may result in a dispensing apparatus that for weeks of shifts.
-
- The Data: Upon actuation, the microprocessor pulls the exact Date and Time from an onboard Real-Time Clock (RTC) and performs a local write to a non-volatile ledger.
- Dispensing apparatus 20 provides at-the-source temporal attribution, ensuring 100% data integrity regardless of network status.
- Dispensing apparatus 20 uses asynchronous NTP (Network Time Protocol) Scrubbing. During the physical handshake, the secure physical interface gate (e.g. Raspberry Pi gateway) validates the wearable's local RTC logs against global atomic stratum servers. This provides forensic accuracy-even if the hospital computer is wrong, the hub “scrubs” and corrects the data to ensure absolute legal certainty for Bill S-5 audits.
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- Zero Wireless Footprint: The device has no Wi-Fi™, Bluetooth®, or RFID broadcasting capabilities. It is invisible to hospital wireless networks, eliminating interference and security breaches.
- Physical Handshake: Data offload occurs exclusively via a multi-purpose USB-C port. This port handles both high-speed “Burst” data synchronization and charging. The device connects to a local gateway (e.g., a Raspberry Pi-based hub) which then offloads via hardwired Ethernet.
- Dispensing apparatus 20 physically removes the radio, comprising “air-gapped vault” with zero-RF footprint. Data movement is restricted to a Physical Handshake via a multi-purpose USB-C port. This eliminates the two biggest hurdles in modern healthcare: cybersecurity breaches and RF interference with sensitive ICU/ER equipment (like pacemakers or ventilators).
-
- Efficacy: The device is mechanically calibrated to deliver a single, clinically sufficient dose per actuation for total hand coverage.
- The Performance Metric: Because the power load is event-driven, the device is rated for 500 to 1,000 discrete dispensations per charge. At a spec of 40 doses (one cartridge) per clinician shift, the maintenance/handshake window is reliably predictable (12 to 25 shifts).
- The microprocessor is calibrated to only commit a log to the non-volatile vault if a full mechanical displacement occurs (representing a clinically sufficient dose). This transforms the device from a “counter” into a Validated Clinical Instrument. It proves 100% hand coverage efficacy per log, rather than just “button pushes.”
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- Verification: To eliminate the unreliability of wireless user-tracking, each device's unique Serial Number is manually associated with the user's ID in the administrative database. This 1:1 hardware-to-human link is foolproof for legal/clinical audits.
- Manual Serial-Number Marriage - dispensing apparatus 20 is physically associated with a specific user ID in the administrative ledger. Wireless ID tracking is notorious for “cross-talk” (assigning a dose to the wrong person standing nearby).
The system/method as herein described may ensure 100% deterministic attribution—the data is legally tied to the person holding the hardware. The system/method as herein described may thus comprise a vault with a security gate, where the data logging happens in a hardware-Isolated environment (no wireless radios) and can only be accessed via a physical handshake (USB-C). In 2026, hospital IT directors may not allow wireless “data sharing” because of ransomware risks. The system/method as herein described is not merely data sharing, but may be said to comprise a secure transfer protocol that protects the hospital's core infrastructure from outside interference.
For the asynchronous validation step (e.g. performed by the Raspberry Pi hub), the “logging event” is not finished when the wearable writes the file; it is only complete once the hub scrubs the data, validates the NTP (Network Time Protocol) timestamp, and
converts it into a medical-grade packet (HL7/FHIR). This methodology produces forensic evidence that can be used for Bill S-5 federal compliance audits. The system/method as herein described may thus result in verified clinical events.
The microprocessor rejects the log entry unless the physical plunger travels 100% of its calibrated distance, logging a successful hand hygiene application, which may be said to comprise a legal compliance record.
The system/method thus provides:
-
- 1. Hardware Isolation-Removing the Risk of Wireless Data Exfiltration.
- 2. Temporal Validation-using a local hub to ‘scrub’ and certify timestamps against atomic time.
- 3. Mechanical verification-requiring a physical-logic handshake before a log is authorized.
The Raspberry Pi Hub may be referred to as a trusted execution environment comprising a physical security gate. The port of dispensing apparatus 20 may function as a dual-purpose handshake interface: 1) it transfers data; and 2) it is the exclusive physical key required to unlock the data vault. By removing all wireless radios, dispensing apparatus 20 has turned the port into the sole point of vulnerability control. The data sharing event is not “plug and play”: it requires a hardware-to-hardware authentication between the wearable and the Raspberry Pi Hub. The Raspberry Pi acts as a “Trusted Execution Environment” (TEE): it does not just receive data; it scrubs and validates the logs against NTP (Network Time Protocol) before the port allows the data to move. The port may be said to comprise a physical interface that is electronically isolated from the non-volatile memory (the vault) until a specific cryptographic handshake is completed.
It is therefore intended that the following appended claims and claims hereafter introduced are interpreted to include all such modifications, permutations, additions, omissions, and sub-combinations as may reasonably be inferred. The scope of the claims should not be limited by the preferred embodiments set forth in the examples, but should be given the broadest interpretation consistent with the description as a whole.
Claims
1. A dispensing apparatus comprising:
- a housing having an outlet;
- a rigid or semi-rigid replaceable cartridge having an interior shaped to receive a liquid therewithin and an opening via which the interior is accessible;
- an elastomeric sealing element which couples to the cartridge and covers said opening;
- a piercing element that pierces through the elastomeric sealing element when the cartridge is inserted into the housing; and
- a metering mechanism fluidly connected to the piercing element and the outlet, the metering mechanism operable to draw the liquid from the cartridge so inserted into the housing, to the outlet, wherein operation of the metering mechanism to dispense the liquid generates a negative pressure within the cartridge, and wherein the elastomeric sealing element deforms in response to the negative pressure to allow air to enter the cartridge via the opening as the liquid is removed therefrom.
2. The dispensing apparatus of claim 1, wherein the sealing element includes a generally tubular body coaxial with said opening and a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element; and wherein one or more of: the central membrane is positioned within the interior of the cartridge; and/or wherein the central membrane has a thickness that is generally less than that of the tubular body and/or decreases from a periphery thereof towards a center thereof.
3. The dispensing apparatus of claim 1, wherein the sealing element has a longitudinally-extending exterior which tapers in a direction extending from an outer end portion towards an inner end portion thereof and/or wherein the sealing element is rotationally symmetric about a longitudinal axis thereof.
4. The dispensing apparatus of claim 1, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the sealing element includes a first flange shaped to abut with an interior surface of the cartridge, a second flange shaped to abut an exterior surface of the cartridge, the first and second flanges coupling to and extending radially outwards from the tubular body of the sealing element, with each said flange spanning a lateral extent greater than of said opening, and with the sealing element coupling to the cartridge at least in part via said first flange and the second flange.
5. The dispensing apparatus of claim 1, wherein the sealing element has an inner end positionable within the interior of the cartridge and an outer end positionable outwards from the cartridge, wherein a first flange on the sealing element tapers in a direction extending from the outer to the inner end of the cartridge, wherein a second flange on the sealing element tapers in a direction extending from the inner to the outer end of the cartridge, wherein the first flange and second flange are spaced-apart a distance equal to or less than a wall thickness of the cartridge adjacent said opening, and/or wherein a central membrane of the sealing element aligns with the first flange of the sealing element.
6. The dispensing apparatus of claim 1, wherein the sealing element has an inner end positionable within the interior of the cartridge, an outer end axially spaced from the inner end thereof and positionable outwards from the cartridge, an outer bore which extends from the outer towards the inner end of the cartridge and an inner bore which extends from the inner towards the outer end of the cartridge, wherein the sealing element includes a laterally-extending central membrane, and wherein the central membrane and/or inner bore are adjacent the inner end of the cartridge.
7. The dispensing apparatus of claim 6, wherein the sealing element includes an inner annular surface which extends about the outer bore thereof and wherein the sealing element includes an annular portion which couples to and extends radially inwards from the inner annular surface thereof, wherein the annular portion of the sealing element is adjacent the outer end of the sealing element, wherein the annular portion of the sealing element is an isosceles trapezoid in lateral section.
8. The dispensing apparatus of claim 1, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, and wherein the central membrane and/or piercing element are arranged and/or sized so as to enable a sealing force of central membrane exerted on an outer surface of the piercing element to be overcome upon a pressure differential between atmospheric pressure and pressure within cartridge reaching and/or exceeding a set and/or predetermined threshold.
9. The dispensing apparatus of claim 1, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the sealing element deforms to allow air to be drawn into the cartridge at least in part in the form of: the central membrane moving away and/or outwards from the piercing element; the central membrane moving radially outwards from an outer surface of the piercing element; an interior surface of the central membrane becoming outwardly concave and/or more outwardly concave; an exterior surface of the central membrane becoming outwardly convex and/or more outwardly convex; and/or the central membrane moving both longitudinally inwards and radially outwards relative to the piercing element.
10. The dispensing apparatus of claim 1, wherein the sealing element includes a generally tubular body coaxial with said opening, wherein the sealing element includes a central membrane extending across an interior of the tubular body and positioned to be pierced by the piercing element, wherein the membrane so positioned flares outwards in a direction extending from an inner end portion towards an outer end portion of the sealing element, wherein the membrane is biased by the piercing element so as to enclose a first space or passageway which is annular and which tapers in a direction extending from a periphery towards a center thereof, and wherein said deformation creates a temporary second space or passageway which is annular, wherein the second space or passageway is near or adjacent the center of the membrane and is in fluid communication with the first space or passageway.
11. The dispensing apparatus of claim 1 including a mounting assembly comprising:
- i) a mount affixed to the housing including a plurality of mount magnets and a backing plate including a plurality of backing plate magnets, wherein the backing plate is arrangeable relative to the mount so as to align each of the backing plate magnets with a respective one of the mount magnets to thereby magnetically couple the backing plate to the mount; and/or
- ii) an elasticated band operatively connected to the housing and positionable on an arm of a user of the dispensing apparatus.
12. A method of recording actuation data for the dispensing apparatus of claim 1, the method comprising:
- (a) dispensing a volume of fluid from the apparatus in response to actuation of a dispensing mechanism;
- (b) in response to the actuation of the dispensing mechanism, causing a suitably configured processor to record an actuation record in a local memory of the apparatus; and
- (c) transmitting the actuation record from the local memory to a separate external device via a physical port on the apparatus, wherein the actuation record comprises a unique identifier associated with the apparatus and/or a timestamp associated with the actuation of the dispensing mechanism.
13. A replaceable cartridge for a personal dispensing apparatus, the cartridge comprising:
- a rigid or semi-rigid hollow body having an interior within which a liquid is receivable, the body having spaced-apart first and second apertures each in fluid communication with the interior thereof; and
- a membrane coupled to the body so as to cover the first aperture, wherein the membrane inhibits passage of the liquid therethrough, and enables passage of gas therethrough to relieve negative pressure generated when the liquid is dispensed through the second aperture.
14. The replaceable cartridge of claim 13 wherein the membrane is: secured to the body via induction sealing or an adhesive; a thin, microporous membrane; and/or waterproof and breathable.
15. The replaceable cartridge of claim 13 wherein: the first aperture has a diameter generally or substantially equal to less than 1 mm (millimeter); and/or wherein the membrane comprises expanded polytetrafluoroethylene.
16. A personal dispensing apparatus comprising:
- a housing having an outlet;
- a metering mechanism for dispensing a fluid out of the outlet; and
- a valve positioned on a fluid path between the metering mechanism and the outlet, the valve including an obstructing element, a valve seat, a channel, and a resilient member positioned within the channel, wherein the resilient member biases the obstructing element into sealing engagement with the valve seat via a spring force, and wherein fluid pressure from the metering mechanism overcomes the spring force so as to dislodge the obstructing element from the valve seat and thereby permit the fluid to flow around the obstructing element and through the channel to the outlet on the housing.
17. The personal dispensing apparatus of claim 16 wherein: the valve has a valve inlet and a valve outlet, with the valve outlet being smaller than the valve inlet; the valve in part functions as a nozzle and/or wherein the valve is shaped to jet the fluid outwards from the valve outlet thereof; the valve is positioned at the outlet of the housing, with a longitudinal axis of the valve being positioned at a non-parallel angle relative to longitudinal and lateral axes of the housing; wherein the valve (and/or the valve outlet thereof) comprises a last point of contact of the fluid; and/or the valve includes one or more valve bodies which are continuously tubular from proximal to distal ends thereof so as to inhibit passage of fluid radially therethrough.
18. A system for recording actuation data, the system comprising:
- a local device; and
- a personal dispensing apparatus including a dispensing mechanism to dispense fluid, a local memory, a physical port, and a processor, wherein the personal dispensing apparatus records via the processor an actuation record in the local memory in response to an actuation of the dispensing mechanism, and wherein the personal dispensing apparatus transmits via the processor the actuation record from the local memory to the local device via the physical port.
19. The system of claim 18 including one or more of: wherein the personal dispensing apparatus records via the processor a plurality of actuation records in the local memory in response to a corresponding plurality of actuations of the dispensing mechanism to thereby obtain an actuation record set; wherein the personal dispensing apparatus transmits via the processor the actuation record set to the local device; wherein the actuation record comprises a time of the actuation obtained from an onboard clock of the personal dispensing apparatus, a volume of fluid dispensed by the dispensing mechanism, and/or a user identifier; wherein the processor transitions from a low-power sleep state to an active state in response to the actuation to record the actuation record; wherein the actuation record is analyzed via the local device by comparing the time of the actuation to an employee shift schedule; and/or wherein the time of actuation is a preliminary time of actuation, with the local device being configured to concurrently obtain an authoritative time from an authoritative time source, and a current time from the onboard clock of the dispensing apparatus, determine a temporal offset by comparing the current time from the onboard clock and the authoritative time from the authoritative time source, and apply the temporal offset to the preliminary time to generate a certified time of actuation.
20. The system of claim 18 wherein the dispensing mechanism is operable to dispense a volume of the fluid, and wherein the personal dispensing apparatus records via the processor the actuation record only upon: completion of a dispensing mechanism operation cycle corresponding to the configurable, and/or predetermined and/or minimum threshold volume of fluid being dispensed; and/or an actuation time being equal to greater than a predetermined minimum threshold and/or time and/or 1 or 1.5 seconds.
Type: Application
Filed: Mar 27, 2026
Publication Date: Aug 6, 2026
Inventor: Michael WATSON (Hope)
Application Number: 19/632,089
