Abstract: A stethoscope cover having an enclosure with a closed end and an open end. An arrangement (e.g., a circular element) can be located substantially near the closed end can hold a bell of the stethoscope. A V-shaped elastic arrangement can be located at the open end and can extend the enclosure when earpieces of a stethoscope can be pulled apart. A strap can be located at the open and can hold the stethoscope in the enclosure.

Abstract: A surgical instrument holder that can be affixed to a surgical drape and provide a receptacle for holding surgical instrument during an operation. The surgical instrument holder has an elongated hollow body with an outwardly flared top to facilitate inserting an instrument therein. A connection system allows the user to couple a plurality of surgical instrument holders together to facilitate the holding of multiple instruments.

Abstract: An orthopedic fixation system includes a sterile packaged implant kit and a sterile packaged instrument kit. The sterile packaged implant kit includes at least one surgical implant, an insertion device, and an implant package adapted to receive the at least one surgical implant and the insertion device therein. The implant package maintains the at least one surgical implant and the insertion device sterile after sterilization of the sterile packaged implant kit. The sterile packaged instrument kit includes one or more instruments necessary to use the sterile packaged implant kit and an instrument package adapted to receive the one or more instruments therein. The instrument package maintains the one or more instruments sterile after sterilization of the sterile packaged instrument kit.

Abstract: The system according to the present disclosure includes a metal stent (3) as a medical implant for treating lesions in blood vessels and a packaging (1) having an inside volume, in which the stent (3) is arranged in a protected manner. The stent (3) has a plurality of webs (33), which produce a tubular shape with each other, and a proximal end (31) and a distal end (32), between which a stent lumen (34) extends. The stent surface (35) has a hydrophilic property. The molecular chemical impurities originating in the atmosphere, primarily hydrocarbon compounds, are significantly reduced on the surface by a treatment, whereby the contact angle as a measure of the hydrophilicity of a water drop present on the surface (35) is reduced in proportion to the contact angle prior to said treatment. The stent (3) is stored in an inert manner in the packaging (1).

Abstract: A film is mated with a paper to form a space therebetween. The film is made of plastics material. Separation of the paper from the film can provide access to an article stored in the space provided between the paper and the film.

Abstract: A container having a base and a cap is disclosed herein for protecting needles and/or catheters during transport. The base has a cavity for storing the needle and/or catheter and a flange region for securing the needle and/or catheter within the base. The cap can be releasably coupled to the base and provide a seal to protect the needle and/or catheter from contamination. Semi-permeable plugs can be disposed on the ends of the base and cap to enable gas sterilization of the container and the needle and/or catheter contained inside.

Abstract: An apparatus for storing a defibrillator, such as an AED, on a host structure includes a container shell mountable to the host structure. The container shell may be used to store the defibrillator within it. Also included in the container shell is a vibration-dampening material disposed between the host structure and the housing of the defibrillator. The vibration-dampening material is configured to reduce an amount of vibration of the host structure imparted to the defibrillator. This is especially useful for storing AEDs on means of transportation, i.e. where the traveling host structure is a bus, an airplane, a ship, or an elevator, and where the vibration sources from its propulsion system.

Abstract: Systems and methods that process a plurality of surgical instruments for cleaning and/or packaging. A device identifies a robot-ready insert having a predetermined configuration for accepting at least one type of surgical instrument. The surgical instruments are identified and oriented according to type using an automated apparatus. Specialized tools are also provided for automatically opening and closing surgical instruments, flipping instruments and assisting in the processing and maintenance of surgical instruments. The automated apparatus then places each of the surgical instrument types in one or more predetermined areas of the insert, configured to accept a predetermined set of surgical instrument types.

Abstract: A plastic package for hydrophilic articles, in particular for hydrophilically coated medical instruments, is intended to ensure the hydrophilic nature of the enclosed instrument over a long period of time. The package comprises at least one receiving compartment with a medical instrument for insertion into body tissue and is characterized in that, after sterilization by radiation, it has a proportion of volatile constituents of ?0.1 ?g/cm2.

Abstract: An elongate member housing tool assembly includes a distal end side tubular member disposed on the distal end side and a proximal end side tubular member disposed on the proximal end side, which accommodate an elongate member, and a liquid inlet port to which a liquid supplying tool for supplying liquid into the distal end side tubular member is removably connected and which is provided on the distal end side tubular member. The distal end side tubular member and the proximal end side tubular member are wound spirally, and the proximal end of the distal end side tubular member and the distal end of the proximal end side tubular member are disposed in a spaced relationship from each other. A distal portion of the guide wire is accommodated in the distal end side tubular member, except possibly the most distal portion of the elongate member.

Abstract: A tag for tracking inventory levels and uses of an implant. The tag has a first component having a proximal portion and a distal portion and a second component having a proximal portion and distal portion. Additionally, the tag has an implant receiving cavity formed by the distal portion of the first component and the distal portion of the second component, in which the implant receiving cavity includes an encapsulating extension to substantially encapsulate an implant. Furthermore, the tag has a planar surface formed by the proximal portion of the first component and the proximal portion of the second component. The planar surface extending from the implant receiving cavity is substantially transverse to a longitudinal axis of the implant received within the implant receiving cavity. In addition, the tag has a tamper evident locking mechanism configured for locking the first component to the second component.

Abstract: A catheter assembly includes a catheter, preferably having a hydrophilic surface coating; and a package accommodating said catheter. The package preferably also accommodates a wetting fluid. The package includes a first and a second sheet material connected around the edges; a perforation line extending along a non-closed loop in one of said sheet materials, which defines a flap opening; a third sheet material connected by means of an adhesive over said flap opening. The third sheet material with a margin covers the entire flap opening. The adhesive is adapted to maintain a sterile closure of the package before use, and to be resealable after use. The third sheet material forms a tab not provided with adhesive and the tab provides a grip portion for peel opening of the package.

Abstract: A method for producing a container welded in a protective wrapping, which contains a viscoelastic fluid for use as eye drops in the chirurgical treatment of eyes, wherein the container is configured such that the fluid may be removed from the container via a predetermined breaking point, characterized by the combination of the measures that the viscoelastic fluid is filled into the container, which is thereupon closed, the closed container is welded into a protective wrapping, whereupon the welded container including the protective wrapping is subjected to thermal sterilization.

Abstract: An apparatus includes a container defining an internal region configured to contain multiple medicament delivery devices, such as, for example, pen injectors, auto-injectors, inhalers or the like. The container includes an electronic circuit system configured to output a first electronic output associated with a first medicament delivery device contained within the internal region when the first medicament delivery device is removed from the internal region of the container. The electronic circuit system is further configured to output a second electronic output associated with a second medicament delivery device contained within the internal region when the second medicament delivery device is removed from the internal region of the container. The second electronic output is different than the first electronic output. At least one of the first electronic output or the second electronic output is associated with a use instruction.

Abstract: The present invention relates to a packaging for a medical device comprising a casing adapted to at least partially receive and/or to accommodate the medical device featuring at least one user-driven function, wherein the casing comprises at least one functional element adapted to imitate the at least one function of the medical device.

Abstract: A container (10) is provided for housing a medical accessory (20), such as a valve of a flexible medical endoscope, during processing (cleaning and high level disinfection) thereof following its use on a patient. The container (10) has a closure mechanism (15) comprising first and second complementary members (16, 17) adapted to engage with one another. Once engaged, the first and second complementary members (16, 17) cannot be disengaged from one another without the container (10) breaking. The container (10) is thus suitable only for single use, so as to prevent cross-contamination, and to comply with appropriate public health guidelines.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case is constructed without protrusions and with a rigid handle, which combine to allow easy removal and deployment of the contents from a vehicle storage location to a cardiac arrest patient. The carrying case is further constructed for greater ease of use during rescue, greater ro-bustness, and for ease of maintenance.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case is constructed without protrusions and with an arcuate and semi-rigid or rigid handle, which combine to allow easy removal and deployment of the contents from a vehicle storage location to a cardiac arrest patient. The carrying case is further constructed with a wide angle viewing ready status light pipe for greater ease of maintenance of the contents.

Abstract: The present invention relates to a device for storage of medical equipment. In particular, the present invention relates to a single-use storage device for components of a piece of medical equipment that retains the components with the piece of medical equipment. More particularly the storage device may be used to store endoscope valves, with the parent flexible endoscope. A single-use storage device for medical equipment comprises a container portion, for holding one or more pieces of medical equipment, a closure portion, designed to engage with the container portion to form an enclosure around said medical equipment, a plurality of apertures permitting fluid flow through the storage device, and securing means to secure the closure portion to the container portion, the securing means arranged such that once the closure portion has been secured to the container portion using the securing means the closure portion and container portion cannot be separated without permanently disabling the securing means.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case hinge is constructed for greater structural integrity when the case is open, and to have a flush-mount profile when the case is closed.

Abstract: A collapsible single-use sterilization container for use in the sterilization of medical instruments is provided. The sterilization container includes a lid having central portion defined by a frangible region. Upon activation of the frangible region, the central portion may be removed rendering the sterilization container inoperable for future use.

Abstract: The present invention relates generally to the field of analysis, for example biological analysis.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case is constructed without protrusions and with a rigid handle, which combine to allow easy removal and deployment of the contents from a vehicle storage location to a cardiac arrest patient. The carrying case integrates a actuator to periodically test the operation of the defibrillator push buttons.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case is constructed without protrusions and with a rigid handle, which combine to allow easy removal and deployment of the contents from a vehicle storage location to a cardiac arrest patient. The carrying case is further constructed with a bracket or optional test fixture for a CPR Meter.

Abstract: A package system and method are provided for storing and shipping of elongated endoluminal devices. In one aspect, the system includes a packaging tray having a first area to maintain the position of a first portion of the elongated endoluminal device and a second portion retaining an opposing portion of the elongate device. The second portion configured to hold the coupling element of the assembly and being radially spaced outward from the first portion.

Abstract: A magnetic medical pick up device having a top piece and a bottom piece which removeably engage one another with a cavity positioned between the top and bottom piece. At least one magnetic piece is positioned within the cavity and a handle is connected to the top exterior portion of top piece for handling the magnetic medical pick up device. In use, the top piece and bottom piece are separated from one another, and the top piece is positioned over a contaminated medical device. In this position the magnetic attraction of the magnet pulls the contaminated medical device within the cavity and the bottom piece is engaged with the top piece thereby quarantining the contaminated medical device. As at least a portion of the top piece and/or bottom piece are transparent, the contaminated medical device can be inventoried at the end of the procedure while remaining quarantined within the cavity.

Abstract: A clear, sealable isolation sleeve for use in a medical environment especially with hand-held electronic devices, for the purpose of reducing the spread of infectious diseases. The sleeve offers an isolated containment for such hand-held medical devices while in patient proximity. The sleeve features a perforated tear zone for easy removal and disposal. Embodiments of the present invention can be manufactured from a clear material that allows the hand-held device to read bar codes through it, while also allowing the clinician to read displayed data and manipulate keypads on the device all while contained within the sleeve.

Abstract: A neutral field tray includes a base with a width that tapers from a proximal end to a distal end, and an instrument trough at least partially recessed relative to the base and sized and configured to support at most a single surgical instrument. The trough is obliquely oriented relative to the base so as to present the proximal end of the instrument substantially above the base and to shield a sharp of the instrument within the trough. The tray also includes supporting structure for supporting the tray relative to a supporting surface.

Abstract: The ostomy receiving bag comprises a front wall (2) and a rear wall and has a top end and a bottom end. The top end of the rear wall is provided with an inlet to receive a stoma, and one wall is provided with at least one first half of a fixation pair (A), and the same effective wall after closure of the bag, if available, is provided with at least one second half of a fixation pair (B), such that when the first half and the second half of the fixation pair are attached, the volume of the receiving bag is reduced.

Abstract: A method is provided for storing a medical device. One step of the method includes providing a medical device having an initial tensile strength. The medical device is placed into a storage container so that at least a portion of the medical device is immersed in a hydrophobic liquid. Next, the medical device is stored in the storage container for a period of time. The initial tensile strength of the medical device is substantially preserved over the period of time.

Abstract: The present invention is directed to a container suitable for use in the disinfection of blood glucose meters and other medical devices. In one embodiment, the container comprises a tray with a formed cavity in it, such that a blood glucose meter or medical device may be placed and retained in it. In certain related embodiments, the meter has been wrapped in a disinfection wipe prior to placement into the container.

Abstract: A storage receptacle for storage of a medical instrument such as an endoscope comprises a base and a plurality of upstanding walls extending from the base defining an enclosure for receiving and storing a medical instrument. A cover member is provided for closing the enclosure. The cover member comprises a first indicia provided on a first face indicative of an unused condition and a second indicia provided on an opposing face of the cover indicative of a used condition and the cover member is configured to attach to and close the enclosure in a first orientation in which the first face is outwardly facing and in a second orientation in which the second face is outwardly facing. The storage receptacle therefore permits the sterile condition of the contents to be readily discerned by the user and prevents dirty instruments from being returned to storage in an unsterile condition.

Abstract: A package for containing a medical device can have a bottom portion and inner and outer lids releasably sealed to the bottom portion. The bottom portion defines a cavity for receiving a medical device. A flange extends outward from sidewalls of the bottom portion and includes an inner flange portion and an outer flange portion. The inner flange portion can be recessed below the outer flange portion. The sealed inner lid permits sterilization of the cavity. The outer lid provides a moisture-resistant barrier to the package. A corner portion of the outer lid can extend past a corner of the bottom portion. Upon application of a withdrawing force sufficient to break the seals, the inner lid and the outer lid are together capable of being peeled from the bottom portion.

Abstract: A securement device for securing a catheter to a patient is provided. The securement device includes a base including a support member and at least one securement arm extending away from the support member. The support member defines a cradle portion, the cradle portion of the support member being configured to receive at least a portion of a catheter. The at least one securement arm being movable over the cradle portion to a position to secure a catheter within the cradle portion. The securement device further includes a cover member configured to be received over the base and dimensioned to secure the base to a patient.

Abstract: A package for a medical device having a handle and an elongated shaft. The package includes a holster for holding the medical device, the holster having a tubular member for receiving the elongated shaft and a handle cover located at a proximal end thereof. The handle cover has a holster opening for accessing the handle to draw the medical device from the holster. The package includes a pouch having a sealed area bounded by a top sealed edge, a bottom sealed edge, a pair of side sealed edges extending between the top and bottom sealed edges, and at least one opening tab spaced from the bottom sealed edge. The medical device and the holster are disposed within the sealed area of the pouch with the elongated shaft of the medical device extending along the bottom sealed edge and the holster opening being located adjacent the at least one opening tab.

Abstract: Certain aspects of the invention are generally directed to devices for withdrawing a substance from the skin and/or from beneath the skin of a subject, and/or for delivering a substance to the skin and/or to a location beneath the skin of a subject. In some embodiments, the devices may comprise one or more skin insertion objects, such as needles or microneedles. In some cases, the device also may comprise one or more vacuum chambers. In some aspects, the device may be contained within an environment able to assist with maintenance of such pressures. For example, a package containing such an environment may also have a pressure less than atmospheric pressure, and/or the package may be molded to the device or otherwise have a shape that does not contain substantial gases that can “leak” into the device and alter the pressure of any vacuum chambers that may be contained therein.

Abstract: A surgical instrument securing device is provided for holding medical instruments. The surgical instrument securing device may be formed from a silicone, rubber, or other polymer based base and may be elastomeric. Slots in the base may define one or more substantially arcuate, circular, elliptical, or other geometrically shaped spaces within the base which open towards at least one side of the base, wherein one or more surgical instruments may be secured by inserting a portion of the instrument into one of the slots. A method for securing surgical instruments is also provided wherein surgical instruments are secured by inserting a portion of the instruments into the slots within the silicone or other polymer based base.

Abstract: A grommet device and method of using a grommet device is provided. The device includes a base structure having a base surface and a top structure having a top surface. A middle portion is connected between the top structure and the base structure, wherein an aperture is positioned through the middle portion, the aperture having an interior space defined by an aperture sidewall extending from the base surface to the top surface. A protruding structure is affixed to a portion of the aperture sidewall at a first end and extending towards a central axis of the aperture along a protrusion axis, wherein the protrusion axis is substantially aligned with a length of the protruding structure from the first end to the second end, and wherein a second end of the protruding structure is flexibly movable in at least one direction substantially perpendicular to the protrusion axis.

Abstract: A built-in non-verbal compact instructional device integratable to an applicator having a microdevice for painlessly perforating skin and optionally an active agent for application to the perforated area. The microdevice can include microneedles, microneedle arrays, microblades, microblade arrays, microknives, microknife arrays, and Functional MicroArrays (FMAs). The active agent can be stored in a first chamber. The microdevice can perforate stratum corneum without significant pain or discomfort to a patient. The active agent is applied to the perforated area. The device verifies compliance with predetermined methods of use, such as a light to indicate application with the recommended amount of force for perforating skin. The applicator can provide enhanced delivery of an active agent, with minimal discomfort, for therapeutic or cosmetic treatment, such as topical treatment for acne, or other skin disorders, wrinkles, blemishes, etc.

Abstract: A pouch is formed from one or more webs of material that provide at least one absorbent surface. The pouch further includes an integral flap, which may be folded over the opening, or entrance, of the pouch so as to maintain the contents of the pouch in place and to help retain moisture within the pouch. The interior of the pouch is defined, at least partially, by its absorbent faces.

Abstract: A biopsy marker delivery device are described. The delivery device can include a relatively flexible hollow tube, a pushing member such as a push rod disposed for sliding with the tube, and at least one marker disposed in the tube. A marker blocking member is disposed distal of the distal most marker, and is disposed at least partially within the hollow tube to assist in preventing premature deployment of a marker from the hollow tube. A portion of the blocking member may disposed in the hollow tube, and another portion of the member may be operatively associated with a portion of the package such that when the marker delivery device is removed from the package, the member is removed from the marker delivery device.

Abstract: A package for containing a medical device can have a bottom portion and inner and outer lids releasably sealed to the bottom portion. The bottom portion defines a cavity for receiving a medical device. A flange extends outward sidewalls of the bottom portion and includes an inner flange portion and an outer flange portion. The inner flange portion can be recessed below the outer flange portion. The sealed inner lid permits passage of sterilization. The outer lid provides a moisture-resistant barrier to the package. A corner portion of the outer lid can extend past a corner of the bottom portion. Upon application of a withdrawing force sufficient to break the seals, the inner lid and the outer lid are together capable of being peeled from the bottom portion.

Abstract: A medicament delivery device includes a housing, a medicament container disposed within the housing, an activation mechanism, a cover and an electronic circuit system. The activation mechanism includes an energy storage member configured to produce a force to deliver the dose of a medicament and/or vaccine. The cover is configured to receive at least a portion of the housing. The electronic circuit system is coupled to the housing such that a protrusion of the cover electrically isolates a battery from a portion of the electronic circuit system when the portion of the housing is received by the cover. The electronic circuit system is configured to be electrically coupled to the battery and to produce a recorded speech output when the portion of the housing is at least partially removed from the cover. The electronic circuit system configured to produce a signal when the activation mechanism is actuated.

Abstract: A method and apparatus for removing and containing a blade from a round scalpel handle comprising a sharps container having a wall portion that defines one side of a containment volume; a slot of a first type having a length and width dimensioned to receive a blade mounted around scalpel handle and prevent its rotation, the slot of the first type formed through the wall portion of the sharps container which slot allows rotation of the handle so the blade becomes disengaged from the handle and disposed in the containment volume.

Abstract: A surgical system includes a surgical instrument, a generator, and a sterilization case. The surgical instrument includes an end effector assembly adapted to connect to a source of energy. The generator is configured to couple to the surgical instrument to supply energy to the end effector assembly of the surgical instrument. The sterilization case is configured to retain the surgical instrument therein and is configured to couple to the generator. The generator is further configured to supply energy to the sterilization case when coupled thereto to sterilize the surgical instrument disposed therein.

Abstract: A storage device is provided for holding bone implant surgery articles. The storage device includes a body defining a plurality of openings capable of holding at least one rotatable drill bit that may be mounted on a drill and used to form a bore in bone and at least one implant container that holds an implant capable of being placed in the bore.

Abstract: An apparatus includes a medicament container and a package. The medicament container includes a wall configured to define a medicament reservoir. The wall includes a protrusion configured to propagate a deformation of the wall when an external force is applied to the protrusion to reduce a volume of the medicament reservoir. The package includes a blister portion and a foil portion and defines a cavity therebetween. The blister portion is configured to cover the medicament reservoir when the medicament container is disposed within the cavity.

Abstract: A tray and packaging system for a prosthetic valve delivery system permits conversion from a storage and/or shipping configuration to a set up and preparation configuration. In a first configuration, a delivery system can be supported by first and second main trays with the elongate catheter of the delivery system arranged to extend linearly from the first main tray to the second main tray, and in a second configuration, the delivery system can be supported by the first and second main trays with the elongate catheter of the delivery system turned back in a U-shaped manner with the deployment portion of the delivery system positioned to the side of the control handle portion of the delivery system.

Abstract: A package for containing a medical device can have a bottom portion and inner and outer lids releasably sealed to the bottom portion. The bottom portion defines a cavity for receiving a medical device. A flange extends outward sidewalls of the bottom portion and includes an inner flange portion and an outer flange portion. The inner flange portion can be recessed below the outer flange portion. The sealed inner lid permits passage of sterilization. The outer lid provides a moisture-resistant barrier to the package. A corner portion of the outer lid can extend past a corner of the bottom portion. Upon application of a withdrawing force sufficient to break the seals, the inner lid and the outer lid are together capable of being peeled from the bottom portion.

Abstract: A processes of sterilizing a contact lens, that is immersed in an aqueous liquid and hermetically in a container, using at least 284 mJ/cm2 of UV radiation in the range of 240-280 nm is disclosed herein.