Abstract: A sample collection container adapted to be connected to, and disconnected from, a sample collection adapter and a sample collection container cap. The sample collection adapter has a downward sloping interior surface that provides a free-flowing path for samples provided by a subject to the sample collection container. The sample collection adapter may have a three-dimensional rim that is curved in two different non-parallel planes.

Abstract: A blood glucose meter includes a front attachment part to which a test piece is attached, a measurement part for measuring a component of blood collected via a blood guide passage in the test piece, and a monitor for displaying the measurement results obtained by the measurement part. When the device is placed on a horizontal plane by referring to the display face of the monitor as the upper side and the opposite side as the lower side and placing the display face of the monitor upward, the central axis of the test piece extends obliquely downward toward the front side. The blood glucose meter comprises a main part provided with the monitor and a linking part between the main part and the front attachment part. The top face of the linking part is placed roughly parallel to the central axis line and is provided with an ejector lever.

Abstract: A portable laser blood sampling device equipped with a dual safety device and a disposable cap used therewith are provided. Specifically, a portable laser blood sampling device equipped with a dual safety device which enables safe laser irradiation when a laser is irradiated to the outside by a laser module and a disposable cap used therewith are provided.

Abstract: A device includes a pre-sample reservoir, an actuator mechanism, and a diverter. The pre-sample reservoir can be fluidically coupled to a delivery member to receive and isolate a predetermined volume of bodily-fluid withdrawn from a patient. The actuator mechanism is operably coupled to the pre-sample reservoir such that, when actuated, a negative pressure is formed in the pre-sample reservoir that urges the bodily-fluid to flow into the pre-sample reservoir. The diverter can selectively control fluid flow between the delivery member and the pre-sample reservoir. The diverter includes a flow control mechanism that defines a first fluid flow path and a second fluid flow path. The diverter is movable between a first configuration in which the bodily-fluid flows through the first fluid flow path to the pre-sample reservoir, and a second configuration in which the bodily-fluid flows through the second fluid flow path to a sample reservoir coupled to the diverter.

Abstract: A portable system for subatmospheric pressure therapy in connection with healing a surgical wound, includes a wound dressing dimensioned for positioning relative to a wound bed of a subject, a portable subatmospheric pressure mechanism dimensioned to be carried or worn by the subject and a container for collecting exudates from the wound bed removed under the subatmospheric pressure supplied by the subatmospheric pressure mechanism. The portable subatmospheric pressure mechanism includes a housing, a subatmospheric pressure source disposed within the housing and in fluid communication with the wound dressing to supply subatmospheric pressure to the wound dressing and a power source mounted to or within the housing for supplying power to actuate the subatmospheric pressure source.

Abstract: Device for semen collection from boars consisting of a grip strip and a clamping fixture for a detachable fixing of the grip strip placed around the boar penis in a way that the necessary pressure for the ejaculation is exerted by the fixed grip strip.

Abstract: In one aspect, a diagnostic test system includes a receptacle, optical detectors, and a logic circuit. Each of the optical detectors has a corresponding view in the receptacle and produces an electrical signal at a respective detector output in response to light from the corresponding view. The logic circuit includes logic inputs that are respectively coupled to the detector outputs and that produce an output logic signal corresponding to a logical combination of signals received at the logic inputs. In another aspect, respective detection signals are produced in response to light received from respective ones of multiple views of the test strip, and at least one output logic signal corresponding to a respective logical combination of the detection signals is generated.

Abstract: The present invention provides for a device and a kit for collecting body fluids. The device includes a body fluid collection portion comprising a body fluid absorbing material. The body fluid connecting portion has a free edge and is hingedly connected at the edge opposite to the free edge to a first support panel and a second support panel. A base panel is hingedly connected to the first support panel or the second support panel. In a first folded condition the body fluid collection portion is sandwiched between the first support panel and the second support panel in a substantially face contacting relationship.

Abstract: A non-penetrative vacuum blood container for storing blood sample, the non-penetrative vacuum blood container comprises: (a) a cap (1) having a number of air passages (4) at its inner wall and ridges (5) at is outer wall; (b) an enclosure (2) which includes enclosure head (8), enclosure neck (9) and enclosure chamfer (10); and (c) a tube (3) for storing blood sample; wherein the air passages (4) further includes enclosure stopper (7) close to opening (6) of the cap (1); and wherein an enclosure opening (11) is provided at the enclosure head (8).

Abstract: An oral care implement includes a collection system for oral fluids. Some embodiments of the implement may include an oral care region having a wearable oral member having a thickness that is reduced during use, a reservoir for retaining an oral fluid, a receiver coupled to the oral member for receiving an oral fluid, and a fluid pathway in communication with the receiver to provide the oral fluid to the reservoir.

Abstract: A device (1410) for collecting a blood sample from an animal has a holder for holding a sampling media (1456), one or more spikes (1418) that first pass through the sampling media (1456) and penetrate into the flesh of the animal to create a puncture site to allow blood emerging from the site to be collected by the sampling media (1456) during and/or after penetration of the flesh. The device has a retainer (1427) for temporarily retaining the device (1410) on the animal whilst blood is collected and for allowing the device (1410) to be removed from the animal substantially intact for subsequent removal of the sampling media (1456) from the device.

Abstract: A lancet integrated test element tape includes a plurality of lancet integrated test elements. The lancet integrated test elements each include a lancet configured to form an incision in tissue and a test element configured to analyze body fluid from the incision in the tissue. A cartridge includes a supply compartment configured to store an unused section of the tape. The tape is folded within the supply compartment to limit damage to the lancet integrated test elements. The cartridge can further include a waste compartment in which a used section of the tape is stored. An indexing mechanism moves the tape between the supply and waste compartments.

Abstract: A method for sampling and/or introducing a matter to an environment comprises introducing a first array of plugs through a first microchannel of a device into an exchange region of the device in which mass transport between the environment and the plug fluid of at least one plug in the first array of plugs occurs and a second array of plugs is formed. The exchange region is in fluid communication with the first microchannel. The method further comprises directing the second array of plugs into a second microchannel downstream of and in fluid communication with the exchange region.

Abstract: A device for interstitial fluid extraction, having a base material formed from a synthetic resin film, a pressure sensitive adhesive layer, a hydrogel layer formed from at least one hydrophilic polymer selected from the group consisting of polyvinyl alcohol and polyvinyl pyrrolidone, and a release layer, wherein the hydrogel layer has an area of a size that the pressure sensitive adhesive layer is exposed from around the hydrogel layer, does substantially not contain a sodium ion and causes no water separation.

Abstract: A needle assembly includes a transparent or translucent housing with a fluid inlet and outlet end, a flashback chamber, and a venting mechanism therebetween. The venting mechanism includes a blocking member to control the fluid flow in the venting mechanism so that it flows along the longest path through the vent. Substantially axially aligned inlet and outlet cannulas extend from the housing and communicate with the chamber. A sealable sleeve covers the external end of the outlet cannula. Relative volumes of the cannulas, the chamber, and the sleeve are selected to provide rapid reliable flashback indicative of venous entry with an internal vent positioned within the housing to divide the interior into first and second chambers, with the second chamber being adapted to maintain a negative pressure therein relative to the external environment so as to inhibit leakage of blood from the needle tip on withdrawal from the patient.

Abstract: An apparatus for generating and collecting saliva samples containing enhanced cell concentrations includes a mouthpiece having a mouth contact portion and a flow channel which may include a tapered basin, a conduit in fluid communication with the flow channel, and one or more collectors couplable to the conduit. The mouth contact portion and basin may be textured to enhance cell removal. The mouth contact portion may include a plurality of internal and external channels disposed around the flow channel. Filters may be included between the flow channel and the collectors. A closure member is provided.

Abstract: In a syringe type pump with a barrel (2) and a piston (4) movable in the interior of the barrel the barrel has the shape of a segment of a toroidal tube (2) and the piston is moved by means of a driving rod (6) which is guided and supported by the inner surface of the barrel wall. By the toroidal shape the overall size of the pump is significantly reduced and by guiding and supporting the driving rod of the piston by the inner surface of the barrel wall intrinsic problems of tightness, stick-slip phenomena and blockage are solved. A device for injecting fluid into a patient's body or removing body fluid therefrom is using a syringe type pump with a toroidal barrel and a driving rod of the piston guided and supported by the inner surface of the barrel wall.

Abstract: System to improve the quality of blood sample obtained from the foot of an infant specially a newborn baby. The system includes a disposable heatable booty that allows the vessel dilation without massage, friction or pressure, and without injuries or burns. Samples of blood improve in quality and quantity, avoiding the multi-puncture of the foot of the infant, to prevent suffering on the infant and facilitating the work of the personnel performing the extraction.

Abstract: Provided are a decompression mechanism capable of performing a desired pressure reduction by simple operation and having improved operability, a puncture device, a blood analysis device, and a sensor mounting mechanism. A needle puncturing device includes: a piston having at one end thereof an end part for forming a part of a sensor mounting mechanism and at the other end an end part for slidably supporting a rod of a lancet section; a cylinder for slidably containing therein the end section of the piston; and packing mounted to the inner periphery of the end part of the piston and maintaining the air-tightness of the outer periphery of the rod. When the piston is moved in the direction toward the cylinder with a skin contact part in contact with the skin, the volumes of an internal space and a pressure reduction chamber are increased to produce a reduced pressure.

Abstract: Disclosed is a disposable absorbent product for use in testing for the presence of a medical condition, comprising a disposable diaper having a top flap formed of a liquid permeable layer and attached to the diaper on three sides, thereby forming a pocket. The pocket is designed to securely hold an absorbent pad containing a test strip in the crotch region of the diaper. The pocket enables the test strip to come into direct contact with urine or other bodily fluids released by a user in order to detect the presence of a medical condition. A variety of testing protocols can be used based on the expected medical issue, thereby providing a convenient and inexpensive means of detecting a medical condition. The device is particularly useful for patients who suffer from incontinence, mobility impairment, and dementia.

Abstract: The invention concerns a test device, in particular for blood sugar tests, comprising a lancing element which is provided with a lancing component for producing a skin puncture, and a protecting element shielding the lancing element at least in the area of the lancing component. According to the invention it is proposed that the lancing element has a collecting structure for collecting body fluid from the skin puncture and that the protecting element comprises a protecting foil to cover the collecting structure and a holding body for holding the protecting foil on the lancing element.

Abstract: Appurtenances to wound dressings can include: a substrate configured to attach to a wound dressing; a fluid-activated voltaic cell attached to the substrate; a transmission unit attached to a surface of the substrate, the transmission unit including circuitry and at least one antenna, the transmission unit configured to transmit a signal in response to current generated by the fluid-activated voltaic cell; and a projection operably attached to the fluid-activated voltaic cell, the projection of a size and shape to extend into an interior region of the wound dressing and configured to sample a fluid within the interior region of the wound dressing.

Abstract: Appurtenances to wound dressings are described, which include: a substrate configured to mechanically or chemically attach to a wound dressing; a transmission unit attached to a surface of the substrate, the transmission unit including circuitry and at least one antenna, the transmission unit configured to transmit a signal; and a projection operably attached to the transmission unit, the projection of a size and shape to extend into an interior region of the wound dressing and configured to sample a fluid associated with a wound.

Abstract: Disclosed is a set for determining whether blood obtained in puncture tools by puncturing a blood vessel is venous blood or arterial blood easily, and ensuring handling under a sterile state. A set for determining blood type has a cover body to be attached to a syringe set, and a blood type determination unit to be housed in the cover body. The blood type determination unit comprises a light projecting portion and a light receiving element, and a blue output LED and a red output LED showing a judgment result based on a signal obtained from the light receiving element. The cover body has a body and a lid that are combined with each other to cover the blood type determination unit, a partition for passing blood between the light projecting portion and the light receiving element, and a pair of measurement windows for transmitting light between the light projecting portion and the light receiving element through the partition.

Abstract: A sensor and a lancet are integrated with each other. A thin strip-shaped sensor and a lancet are integrated so that the lancet moves in parallel, along a longitudinal direction of the sensor. A measuring device to which an integrated lancet and sensor is attached is provided with a function of driving the attached lancet.

Abstract: An embodiment is a fluid sample collection system. More specifically, an embodiment is a fluid sample collection system to facilitate collection of biological specimens and particularly to facilitate collection of saliva, urine, and stool specimens from human or animal species for the purpose of extracting purified DNA and/or RNA.

Abstract: A urine shield comprises an elongate base and side walls connected to the base. At least one of the sides and base is absorbent. The shield further comprises at least one attachment tab for releasably attaching the shield to a user's skin The shield has an hourglass shaped cross-section. A method and device for the collection of a urine sample from an individual is also provided.

Abstract: A cartridge for an automated blood sampling system for collecting samples and a method of sampling fluids from a test subject using an automated blood sampling apparatus including a cartridge are disclosed.

Abstract: Various methods, devices and systems for patch based physical, physiological, chemical, and biochemical sensors that diagnose and monitor disease states are described. The patch based sensors provide a panel of specific analyte parameters that determine one or more physiological conditions and/or the level of healing progression of a wound. The use of such analyte panels in local or remote monitoring of parameters related to various disease states is also described.

Abstract: An apparatus includes a housing, a flow control mechanism, and an actuator. At least a portion of the flow control mechanism is movably disposed within the housing. The apparatus further includes an inlet port and an outlet port, and defines a fluid reservoir. The outlet port is fluidically coupled to a second fluid reservoir and is fluidically isolated from the first fluid reservoir. The actuator is configured to move the flow control mechanism between a first configuration, in which the inlet port is placed in fluid communication with the fluid reservoir such that the fluid reservoir receives a first flow of bodily-fluid, and a second configuration, in which the inlet port is placed in fluid communication with the outlet port.

Abstract: Instrument for producing a sample of body liquid for analysis by piercing the skin with a lancing element having a skin piercing tip. The instrument has a housing and a lancing drive for driving a lancing element connected thereto in a puncturing movement. A pressure ring surrounds a skin contact opening and is adapted for pressing against the skin such that the skin bulges into the opening for promoting expression of body fluid. The skin contact opening has an opening area corresponding to a circle with a diameter of at least 3 mm and at most 8 mm, and the instrument comprises a pressing force control device for controlling the pressing force between the pressure ring and the skin at the time of triggering the puncturing movement, to be at least 3 N and at most 8 N.

Abstract: A method for conducting a fecal examination includes providing a collection spoon and a collection container comprising a transparent body having a cap which can be removed to permit fecal matter to be received in the collection container with the spoon to be mixed with a flotation material to aid in separating the fecal matter and ova or eggs of parasites that may be contained in the fecal matter and then dispensed through a filter mounted in the cap of the collection container to a test tube and a cover slip on the test tube for examination of the filtered material for the presence of the ova of parasites.

Abstract: A placental blood extractor consists of an outside box having plurality of plastic bags for compressing the placenta and mounted to the top of the box. The lower part of the box has possibility to use several different circularly movable plates for mechanically facilitating the flow of the blood in the collecting veins on the fetal side of the placentas toward the central main umbilical cord vein. The box has an opening in the central lower part of the box and the lower area mechanical tray for the umbilical cord to exit the box. Blood is collected from umbilical cord and is to be collected into commercial collection bags. The area of the bag for collection of blood may be under negative pressure to facilitate the collection of blood but also gravity force may be used for that purpose. Both, the first part with the compression chambers as well as the second part, the Collector of Blood have pumps and manometers controlled by computer in their operations.

Abstract: A vacuum blood collection tube (100) comprises a bottomed tube (101) composed of a low temperature resistant material that is less susceptible to low temperature fracture when cryopreserved at ultra-low temperature, a stopper (102) having a needle piercing portion (113) composed of a rubber material that can be pierced with a blood collection needle (110), and a cryopreservation cap (103) composed of the low temperature resistant material. Before blood collection, the stopper (102) is attached to the bottomed tube (101) to maintain the reduced pressure state inside the bottomed tube (101). Thus, blood collection by a vacuum blood collection method is possible. After blood collection, the cryopreservation cap (103) is attached to the bottomed tube (101), so that the liquid tight state of the bottomed tube (101) is maintained, and cryopreservation at ultra-low temperature as it is possible.

Abstract: A point of care fluid testing system for determining properties of a fluid comprises a patient connection, a primary fluid routing portion, a pump, a secondary fluid routing portion, and a flushing fluid connection. The patient connection connects the system to a patient. The primary fluid routing portion has a pump region, a fluid transfer region, and an in-line testing region. The pump region pumps the fluid sample from the patient to the testing portion and back to the patient. The in-line testing region evaluates a first characteristic of the fluid sample. The fluid transfer region transmits a portion of the fluid sample out of the primary fluid routing portion. The secondary fluid routing portion includes an off-line testing portion that receives the portion of the fluid sample transmitted from the fluid transfer region. The off-line testing portion evaluates a second characteristic of the fluid sample.

Abstract: Sensor apparatus (1) for determining at least one biochemical function of a fluid (F) with at least one magnetoelastic capillary tube (2) through which the fluid (F) is conveyed, wherein a resonant frequency (fR) of the magnetoelastic capillary tube (2), which depends on a surface loading of the inner wall of the magnetoelastic capillary tube (2) by the fluid (F) conveyed through the tube is able to be read out in a non-contact manner for determining the biochemical function of the fluid (F).

Abstract: A kit is provided for gathering biological specimens. The kit generally comprises a self-contained specimen gathering device including a protective housing and a preservation solution. Also provided is a method of gathering specimens and a holistic method of deterring crime using the kit.

Abstract: Systems for and methods of assessing urinary flow rate via sound analysis. Embodiments of the uroflow measurement systems include a computer and a telephone or a digital recording mechanism to capture the sound of one or more urination events, which are stored as audio files in a database. The uroflow measurement systems may include sound analysis software for analyzing the strength and duration of each urination event and may include a web-based uroflow software application for viewing the results via the Internet or other network. In one embodiment, the sound analysis software performs the steps of reading in the raw data of a selected audio file, generating a plot of the audio signal amplitude vs.

Abstract: A flexible container (10) for capturing and or storing saliva, blood or any other body fluid, or biological sample of contained DNA and or other nucleic acid for immediate or later analysis. This bag holds one or more strips (22) assembled from purpose prepared absorbent matrix. A desiccant-containing pouch may be bonded to the interior of the storage device. When the flexible container is manipulated to the open position, the matrix, which is bonded to the interior, becomes exposed. A specimen can then be applied to this matrix. When opened, the bag stands up on its own, allowing the matrix to dry. Upon closure, the air-dried specimen-containing matrix withdraws inside the bag. This flexible container provides in one package, without the need for direct handling of the matrix, a specimen holding means, and protective storage within a substantially airtight, light-proof, and moisture-proof environment for a considerable period of time.

Abstract: A device is provided for blood extraction and collection from the placenta and/or the umbilical cord through a system that combines the collection of the blood falling under gravity, together with a suction system facilitating this fall. Thus, a larger amount of blood can be extracted than is obtained by conventional gravity systems without posing a health risk to the mother, allowing a controlled suction that prevents premature detachment of the placenta.

Abstract: A sample collection implement S1 includes a container 1 having an accommodation portion 10 in which a liquid 5 for suspending or diluting a sample is accommodated, a sample collection stick 2 being able to be disposed in the accommodation portion 10, a filter 3 provided inside the container 1, and a movable member 4 that can be moved in a predetermined direction inside the container 1 and has a function of pushing the liquid 5 and causing the liquid to pass through the filter 3, when moved in the predetermined direction. With such a configuration, when the liquid 5 is filtered, it is not necessary to move the filter 3 by directly pushing it and a filter with a low mechanical strength can be used as the filter 3. In addition, it is not necessary to use a centrifugal apparatus.

Abstract: The present invention provides a method for creating a beveled needle or a blade. The method employs a side wall surface of an angled post as a base to control beveled tip geometry. The invention provides needles, microneedle arrays, blades and microblade arrays with sufficient sharpness and toughness.

Abstract: A method of masking pain resulting from a lancing system can include moving a first portion and a second portion of a lancing assembly in a first direction, stopping the first portion from further moving in the first direction, thereby causing a first vibration, allowing the first portion to move in a second direction while the second portion continues moving in the first direction, and lancing a surface with the first portion while the first vibration is occurring. A system for lancing a surface and masking resulting pain may include a device body having an end adapted to sealingly engage the surface, structure for creating a first portion of a vacuum, structure for causing a vibration, and a lancing mechanism adapted to lance the surface while the first portion of the vacuum and the vibration are acting on the surface.

Abstract: A lancing system can include a device body having a lancing end, a lancing mechanism including a lancing shaft slideably coupled with the lancing end of the body, a main shaft slideably coupled with the body and having an actuating end disposed inside the body, a piston coupled to the main shaft and disposed within the body, a spring coupled to the piston, a release mechanism adapted to selectively couple with the main shaft, and a depth controller removably coupled to the lancing end of the body. A method can include coupling a lance having a needle and a base to the lancing shaft, choosing to use a depth controller having a spacer with a top surface and an opening, engaging a lancing surface with the depth controller, actuating the lancing mechanism, penetrating the lancing surface, and contacting the top surface of the spacer with the base.

Abstract: A flow regulator for a blood collection assembly includes a housing having an inlet and an outlet, which defines an interior space between the inlet and the outlet. A membrane having a first surface and a second surface is disposed at least partially within the interior space. The membrane has a first position where a flow path between the inlet and the outlet is substantially open, and a second position where the flow path between the inlet and the outlet is at least partially restricted. The membrane is configured to move between the first and second positions in response to a pressure differential acting on the membrane.

Abstract: A lancing system can include a device body having a sealing device coupled to a lancing end, a lancing shaft slideably coupled to the lancing end, a lancing spring coupled to the lancing shaft, a release mechanism, a main shaft slideably coupled with a free end of the device body in communication with the release mechanism, a piston coupled to the main shaft, a vacuum spring coupled to the piston, and a shaft coupler having at least two separable portions for removably coupling the lancing shaft to the main shaft. The system can include a lance tool having an insertion portion and a removal portion. A method can include creating a first portion of a vacuum, lancing a surface, and creating a second portion of a vacuum.

Abstract: An apparatus for collecting oral fluid, comprising a vial formed with an inner specimen receptacle for receiving the oral fluid. The open top of the vial is cylindrical and formed with threads on a portion of its outer surface adjacent its open top. The specimen receptacle is disposed within the vial, spaced along its length from the inner surface of the vial and has a closed bottom end and an open top end. The entire periphery of the receptacle top end is sealingly secured to the inner surface of the vial proximal to but spaced from the vial's open threaded end. The bottom end of the vial can be open and flat and extend beyond the closed end of the specimen receptacle to enable the vial to be set on a horizontal surface. A funnel is removably placed in the open top end of the vial and narrows to an inner neck fits within the open top end of the vial.

Abstract: A urine collection system having an elongated shaft with a first end and a second end, a first ring on the first end of the shaft, and a handle on the second end of the shaft, wherein a urine cup is removably held in the first ring, wherein the shaft is rigid, wherein the handle is a second ring, wherein the first ring and the second ring occupy the same planar surface, and wherein the first ring has a diameter larger than that of the second ring.

Abstract: A lancing system can include a device body having a lancing end and a free end, a lancing shaft having an actuating end, a stop coupled to the body, a lancing spring coupled to the lancing shaft, a main shaft having an actuating end, and a shaft coupler having at least two separable portions for removably coupling the lancing shaft to the main shaft, wherein a first portion is coupled to the actuating end of the lancing shaft and a second portion is coupled to the actuating end of the main shaft. A method of extracting blood can include coupling the actuating end of the main shaft to the actuating end of the lancing shaft, moving the lancing shaft toward the free end of the device body, stopping the lancing shaft, uncoupling the actuating ends, and moving the lancing shaft toward a surface to be lanced.

Abstract: A disposable skin-worn device for the transdermal delivery at least one dose of charged therapeutic substances, including granisetron, by iontophoresis, the device comprising a donor reservoir containing an amount of a therapeutic substance to be delivered transdermally by iontophoresis, a counter reservoir, a source of electric power connected in a circuit between the donor reservoir and the counter reservoir and a control system for controlling current flow in the circuit to enable at least one dose of the therapeutic substance to be delivered transdermally by iontophoresis and wherein the control system includes a control element selected from the group consisting of a sensor activated by an external signal and a switch.