Abstract: Bleeding from blood vessels located in difficult-to-compress regions of the body (especially the abdomen, pelvic or groin region) is controlled by the use of a portable, small-footprint belt-like device that contains multiple inflatable bladders. The inflatable bladders are selectively positioned and inflated over exsanguinating blood vessels, thereby exerting pressure to stop the bleeding. The device may also be used to provide perfusion support in low flow disease states such as hemorrhagic shock and cardiac arrest.

Abstract: Bleeding from blood vessels located in difficult-to-compress regions of the body (especially the abdomen, pelvic or groin region) is controlled by the use of a portable, small-footprint belt-like device that contains multiple inflatable bladders. The inflatable bladders are selectively positioned and inflated over exsanguinating blood vessels, thereby exerting pressure to stop the bleeding. The device may also be used to provide perfusion support in low flow disease states such as hemorrhagic shock and cardiac arrest.

Abstract: Bleeding from blood vessels located in difficult-to-compress regions of the body (especially the abdomen, pelvic or groin region) is controlled by the use of a portable, small-footprint belt-like device that contains multiple inflatable bladders. The inflatable bladders are selectively positioned and inflated over exsanguinating blood vessels, thereby exerting pressure to stop the bleeding. The device may also be used to provide perfusion support in low flow disease states such as hemorrhagic shock and cardiac arrest.

Abstract: Bleeding from blood vessels located in difficult-to-compress regions of the body (especially the abdomen, pelvic or groin region) is controlled by the use of a portable, small-footprint belt-like device that contains multiple inflatable bladders. The inflatable bladders are selectively positioned and inflated over exsanguinating blood vessels, thereby exerting pressure to stop the bleeding. The device may also be used to provide perfusion support in low flow disease states such as hemorrhagic shock and cardiac arrest.

Abstract: Provided is a tourniquet having two opposing and pivotally movable plates. The plates comprise a clamp that pinches an elastomeric cord. The plates are pivotally biased together by a spring. The cord is attached to a back end of the clamp. A free end of the cord is squeezed by the plates such that a loop of cord is provided. The cord can be pulled from the clamp to reduce the size of the loop. The clamp comprises a safety lock that prevents movement of the plates and slipping of the cord. The safety lock can comprise a button disposed between the plates in the back end of the clamp, preventing the plates from moving together in the back portion, and therefore from moving apart in a front portion that grips the cord. Also, the tourniquet clamp can comprise a dual-sided press connector mechanism for fast release of tourniquet tension.

Abstract: An apparatus includes a simulated medicament delivery device and an electronic circuit system coupled to the simulated medicament delivery device. The electronic circuit system is configured to output an electronic output associated with a use of the simulated medicament delivery device.

Abstract: An apparatus includes a movable member and a valve coupled to the movable member. The movable member is configured to be disposed within a housing of a medical device and has a first end portion and second end portion. A portion of the first end portion is configured to define a portion of a boundary of a gas chamber. The first end portion defines an opening configured to be in fluid communication between the gas chamber and an area outside the gas chamber. The second end portion is configured to be coupled to a needle configured to deliver a medicament into a body. The valve is configured to selectively allow fluid communication between the gas chamber and the area outside the gas chamber through the opening defined by the first end portion of the movable member.

Abstract: An apparatus includes a label configured to be coupled to a medicament delivery device. The label includes a first surface and a second surface. The first surface is configured to be coupled to an outer surface of the medicament delivery device. The second surface includes a textual indicia. The label further includes an electronic circuit system configured to output an electronic signal.

Abstract: Apparatuses for automatic medicament injection and methods for manufacturing automatic medicament injectors are described herein. In some embodiments, an apparatus includes a housing, a needle, an energy storage member, an actuator, a locking member, and a needle guard. The needle is configured to move between a first position and a second position. In its first position, the needle is contained within the housing. In its second position, at least a portion of the needle extends from the housing. The energy storage member has a first configuration and a second configuration and is configured to produce a force when moving between its first configuration and its second configuration to move the needle from its first position to its second position. The actuator is configured to move the energy storage member from its first configuration to its second configuration.

Abstract: An apparatus includes a housing, a medicament container and an actuator. The actuator includes a release member and an energy storage member having a first position and a second position. In the first position, the energy storage member has a first potential energy. In the second position the energy storage member has a second potential energy. The energy storage member is configured to convert a portion of the first potential energy into kinetic energy when moved from the first position to the second position to move the medicament container within the housing. The energy storage member has a longitudinal axis offset from a longitudinal axis of the medicament container. The release member is configured to selectively deploy the energy storage member from its first position to its second position.

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: Provided is a tourniquet having two opposing and pivotally movable plates. The plates comprise a clamp that pinches an elastomeric cord. The plates are pivotally biased together by a spring. The cord is attached to a back end of the clamp. A free end of the cord is squeezed by the plates such that a loop of cord is provided. The cord can be pulled from the clamp to reduce the size of the loop. The clamp comprises a safety lock that prevents movement of the plates and slipping of the cord. The safety lock can comprise a button disposed between the plates in the back end of the clamp, preventing the plates from moving together in the back portion, and therefore from moving apart in a front portion that grips the cord. Also, the tourniquet clamp can comprise a dual-sided press connector mechanism for fast release of tourniquet tension.

Abstract: Blood clot analysis instrumentation used to evaluate platelet function and clot structure by monitoring force development during clot retraction or upon application of a known amount of force can have a calibration check automatically performed by using a top member with a known amount of mass which is detachable from the instrumentation, and preferably is a disposable component. The calibration check is performed by monitoring force or displacement on a holding member with and without the top member attached. If the difference measured is within a preferred tolerance range, then the instrumentation can be deemed to be within the specifications deemed best suited for the instrument. The top member may also be modified to allow for mixing reagents with the clot, thereby avoiding the need to pre-mix blood with reagents before measurement.

Abstract: Blood clot analysis instrumentation used to evaluate platelet function and clot structure by monitoring force development during clot retraction or upon application of a known amount of force can have a calibration check automatically performed by using a top member with a known amount of mass which is detachable from the instrumentation, and preferably is a disposable component. The calibration check is performed by monitoring force or displacement on a holding member with and without the top member attached. If the difference measured is within a preferred tolerance range, then the instrumentation can be deemed to be within the specifications deemed best suited for the instrument. The top member may also be modified to allow for mixing reagents with the clot, thereby avoiding the need to pre-mix blood with reagents before measurement.

Abstract: A stand is disposed in a heated thermal treatment system basin to support objects placed in the basin above the heated basin floor. The stand may be circular, rectangular or other shape to accommodate various shaped basins and prevent a surgical drape disposed in the basin and containing a heated sterile medium from puncturing. A substantially circular stand includes a substantially circular frame elevating a platform having a plurality of spokes reinforced by a plurality of concentric rings, while a substantially rectangular stand includes a substantially rectangular frame elevating a platform having a plurality of intersecting perpendicular rods to form a grid.

Abstract: A surgical drape for use in a thermal treatment system having an automatic dislodgement mechanism for dislodging congealed liquid is accomplished by a drape having either a coefficient of friction approximately in the range of 0.4-1.0 as measured against steel per ASTM 1983 a metalocine-based olefin film having a flexibility approximately in the range of 10K-12K psi secant modulus measured by ASTM D882, a securing mechanism, or a preformed container portion having ribs or ridges to prevent the drape from being drawn beneath the automatic dislodgement mechanism. The securing mechanisms may be attached to the drape either at the ends of a drape portion hanging down from a top surface of the system, or at a location coincident the top surface of the machine. Further, the securing mechanisms may be separate units disposed on the drape subsequent to disposal of the drape in the basin.

Abstract: A surgical drape for use in a thermal treatment system congealing a sterile medium within a basin and automatically dislodging the congealed sterile medium adhered to the drape adjacent basin walls is accomplished by a drape having a drape portion covering the system housing with part of the drape portion disposed in the basin. The drape may further include a pre-formed container portion fitted to match the contour of, and being disposed within, the basin. The container portion may accommodate various shaped basins and include individual fluted sections, drape deformities, or an inflatable bladder surrounded by the fluted sections for facilitating dislodgement of the congealed medium. Further, the drape or pre-formed container portion may include a substantially annular bladder, or a bladder having a plurality of individually inflatable sections for manipulation of the drape relative to the basin to dislodge the congealed sterile medium.

Abstract: A surgical drape for use in a thermal treatment system congealing a sterile medium within a basin and automatically dislodging the congealed sterile medium adhered to the drape adjacent basin walls is accomplished by a drape having a drape portion covering the system housing with part of the drape portion disposed in the basin. The drape may further include a pre-formed container portion fitted to match the contour of, and being disposed within, the basin. The container portion may accommodate various shaped basins and include individual fluted sections, drape deformities, or an inflatable bladder surrounded by the fluted sections for facilitating dislodgement of the congealed medium. Further, the drape or preformed container portion may include a substantially annular bladder, or a bladder having a plurality of individually inflatable sections for manipulation of the drape relative to the basin to dislodge the congealed sterile medium.

Abstract: Sterile surgical fluid is maintained in one or more temperature controlled basins provided at the top of a cabinet. One or more insulated temperature controlled compartments are formed in the cabinet for storing supplemental supplies of the surgical fluid at the temperatures close to the temperatures of the basins to facilitate replenishing and/or replacing the fluid in the basins. The storage compartments can be used for long-term temperature controlled fluid storage when basin temperature is not being controlled (i.e., between surgical procedures).

Abstract: A surgical drape for use in a thermal treatment system congealing a sterile medium within a basin and automatically dislodging the congealed sterile medium adhered to the drape adjacent basin walls is accomplished by a drape having a drape portion covering the system housing with part of the drape portion disposed in the basin. The drape may further include a pre-formed container portion fitted to match the contour of, and being disposed within, the basin. The container portion may accommodate various shaped basins and include individual fluted sections, drape deformities, or an inflatable bladder surrounded by the fluted sections for facilitating dislodgement of the congealed medium. Further, the drape or preformed container portion may include a substantially annular bladder, or a bladder having a plurality of individually inflatable sections for manipulation of the drape relative to the basin to dislodge the congealed sterile medium.