Abstract: One end of a tubular portion (16) is sealed with a stopcock (5) that is fitted in the tubular portion (16). A first flow channel (33) and a second flow channel (36) are formed in the stopcock (5). A first hole (37), a second hole (43), a third hole (38), and a fourth hole (44) are formed in a connector main body (2). Switching between a setting that brings an inner space (16a) of the tubular portion (16) into communication with the first hole (37) via the first flow channel (33) and a setting that brings the inner space (16a) of the tubular portion (16) into communication with the second hole (43) via the first flow channel (33) and brings the third hole (38) into communication with the fourth hole (44) via the second flow channel (36) can be achieved by rotating the stopcock (5).

Abstract: A wound-closing dressing, which is suitable for use as part of a reduced-pressure, wound-treatment system, may include a sealing drape, one or more contracting elements, and a gripping member. The contracting element may be coupled to the sealing drape and is configured to contract when activated and to generate a closing force. A gripping member is coupled to the sealing drape and is configured to transmit the closing force to a patient's epidermis. Other dressings, systems, and methods are also disclosed.

Abstract: A first connector includes a first connector main body configured from an outer tube of cylindrical shape, an inner tube of cylindrical shape, and a hub disposed at a proximal end portion of the outer tube, a hollow needle supported on the hub, a first sealing member supported on the inner tube, a coil spring serving as puncturing portion biasing means for biasing the first sealing member toward a distal direction, and a clamping member disposed upon the outer tube. Upon an inner periphery portion of the proximal end portion of the outer tube, a pawl is formed so as to project to the inner side. Upon an outer periphery portion of a large diameter portion of a main body portion of the hub, a plurality of ratchet teeth which are engageable with the pawl of the outer tube are formed so as to project toward the outer side.

Abstract: A primary package for simultaneously dispensing microdoses of from 5 to 500 microliters of one medicament contained in a medicated module and another medicament contained in an attached injection system is disclosed, where the primary package contains a single dose of medicament contained within a reservoir cavity sealed with closure caps that secure top and bottom septa.

Abstract: A flexible container receives a liquid material, which is freeze-dried in situ within the flexible container. A gas permeable material that is separate from the flexible container provides gas transport for sublimation during drying and lyophilization. The gas permeable portion of the system can be isolated and removed from the flexible container post-lyophilzation The freeze-dried material is stored in the flexible container until administration is necessary. The flexible container receives a reconstituting liquid for mixing with the freeze-dried material, and conveys the reconstituted freeze-dried material from the flexible container for administration to an individual.

Abstract: A method and apparatus for separation, concentration, and/or applying a biological or bio-engineered fluid. Generally, the fluid application device includes a sprayer body to enable the application of the fluid and a container adaptable to enable the separation of the fluid into at least a first component and a second component. The container is releasably coupled to the nozzle. The nozzle is adapted to withdraw at least one of the first component or the second component from the container after the fluid has been separated to apply the fluid to a selected site.

Abstract: A sampler cap includes a sampler connector, an analyzer connector and a liquid impermeable closure member, which may be a membrane or a filter. The sampler cap may be used to transfer a test sample to an analyzer without removing the sampler cap from the sampler.

Abstract: The blood bag system includes: a blood treating filter for treating a blood; a first bag for containing therein a blood to be supplied to the blood treating filter; a second bag for containing therein the blood treated by the blood treating filter; storage solution supply which supplies a blood component storage solution to the blood treating filter; a third bag into which a blood remaining in the blood treating filter replaced by the blood component storage solution is transferred and in which the recovered blood is temporarily contained; and a fourth bag to which a blood component separated from the treated blood contained in the second bag is transferred and in which the transferred blood component is contained.

Abstract: The invention relates generally to materials for facilitating the administration of dimethyl sulfoxide (DMSO) and related compounds. In one embodiment, the invention comprises a kit comprising items used for the safe and effective administration of DMSO. In another embodiment, the invention relates to indicating containers for holding or delivering DMSO.

Abstract: The invention relates to systems and methods for collecting the content of IV lines that otherwise would be spilt in a hospital environment. In one general aspect the system includes an intravenous tubing system to prevent spillage of fluids. The IV tubing system includes intravenous tubing and a purge bag. The intravenous tubing includes a first end configured to attach to a fluid container and a second end having a connector. The purge bag includes at least one port, such as a needle-free valved port, configured to receive fluids from the intravenous tubing. The purge bag optionally contains a second port is configured to let air into or out of the purge bag with a closing means that may be a needle-free valved port. The purge bag can be packaged separately from the IV tubing set and the package can be opened at the time of use.

Abstract: A dispensing insert is configured to friction fit within a neck of a bottle and to selectively receive an oral syringe. The dispensing insert includes a hollow cylinder, a top plate capping one end of the hollow cylinder, a raised deck extending substantially parallel to and spaced from the top plate, and an annular side wall extending from the top plate upwardly toward the raised deck. The raised deck has a smaller outer diameter than the top plate and defines an opening therethrough configured to provide access to contents of the pharmacy bottle through the dispensing insert. The annular sidewall substantially encompasses an outer perimeter of the raised deck.

Abstract: This disclosure relates to drug vial spikes, fluid line sets, and related systems. In some aspects, a fluid line set includes a frame, multiple spikes extending from the frame, and multiple fluid lines connected to the frame. The frame is configured to hold the fluid lines in a spaced apart configuration.

Abstract: A tube set insertion apparatus for connection to a bottle of saline solution, comprising a flange adapted to connect to the bottle at an opening in the bottle, a plurality of holding members positioned relative to one another to form a channel and to align a drip chamber disposed therein with the opening, each of the plurality of holding members connected to a corresponding one of a rack and a pinion, and a plurality of levers, each lever adapted to rotate about a corresponding pivot, and each lever connected to a corresponding other of the rack and the pinion. Each pinion positioned relative to a corresponding one of the racks such that rotation of the lever about its pivot causes a bottle, when disposed in the channel, to move toward the opening.

Abstract: It is intended to provide an apparatus for separating and storing blood components which facilitates the preparation of serum.

Abstract: An access port for the introduction of a needle cannula tip into an IV tube set includes a rigid tubular housing and a resilient member disposed adjacent an inlet of the housing. The resilient member includes an axial perforation extending through the resilient member, and is normally closed by the resilient character of the resilient member. A depression is defined in a proximal face of the resilient member, and includes sidewalls extending between the proximal face and the axial perforation to guide the tip of the cannulated needle toward the perforation as the cannulated needle is introduced into the access port.

Abstract: A plug for a container capable of improving air-tightness and liquid-tightness is provided. A plug includes a first split piece having a cylindrical first fitting portion to be mounted on an opening portion of a container body and fitted to an opening portion space of the opening portion, an end wall which blocks one end of the first fitting portion, and a first flange portion extending outwardly in a radial direction of the first fitting portion from the other end thereof; and a second split piece having a second fitting portion which is fitted to the first fitting portion of the first split piece and forms a closed space between the end wall and the second fitting portion and a second flange portion extending outwardly in a radial direction of the second fitting portion therefrom.

Abstract: A vial enshrouded or contained in a protective covering which prevents emission of radiation form the vial contents, shielding the environment and personnel from irradiation. The vial optionally has a V-shaped bottom to allow withdrawal of a maximal amount of the fluid without inverting the vial. The vial is equipped with a vial access adapter having a fluid withdrawal spike which extends in to the V-shaped bottom. The vial access adapter may be vented or non-vented.

Abstract: A first connector includes a first connector main body configured from an outer tube of cylindrical shape, an inner tube of cylindrical shape, a hub disposed at a proximal end portion of the outer tube, and a clip disposed so as to be removable at the proximal end portion of the outer tube, a hollow needle supported on the hub, a first sealing member supported on the inner tube, a coil spring serving as puncturing portion biasing means for biasing the first sealing member toward the distal direction, and a clamping member disposed upon the outer tube. In a state in which the clip is mounted to the proximal end portion of the outer tube, a protrusion of the clip engages with a protrusion of the hub, and thereby rotation of the hub is prevented. If the clip is removed, the hub becomes rotatable with respect to the outer tube.

Abstract: A clamp for receiving cylindrical objects, comprising a main body, which on two opposite sides has connecting elements that are matched to one another for detachably connecting similar clamps, and a receiving region, which is designed in a substantially ring segment shape and has a receiving opening for connecting a cylindrical object to the main body in a detachable locking manner, said opening extending over less than 180° of the receiving region, and the inside diameter (D) of the receiving region being 32 mm, 17 mm to 24 mm, or 10 mm.

Abstract: A flexible container for fluid administration is provided having a body defining a cavity, a base, and at least one port comprising a flange in contact with a flange of a terminal port having a punctureable membrane layer. The body has a cross-sectional configuration including a lower body section of a first dimension, a middle body section of a second dimension, and an upper body section of a third dimension, wherein the second dimension is smaller than the first dimension and the third dimension. The flexible container may also include a base having a plurality of creases that are foldable to form two folded ends each including an extension having a base of a first dimension and a tip of a second dimension.

Abstract: Provided is a device for treatment of wounds using reduced pressure, which includes a pump, a gas barrier cover, a first compressible material which expands after compression, and a second material capable of absorbing wound fluids several times its own weight. The first and second materials are arranged inside the cover and form a reservoir connected to the pump. The device also includes an inlet for connecting the reservoir with a wound, a wound pad to be arranged in the wound cavity, and a sealing covering the wound and the wound pad. A third material with high liquid spreading capability is arranged around at least a major part of the first material, and the second material is in the form of at least one layer arranged outside the third material and separated from the first material by the third material.

Abstract: A one-piece bottle is provided, the bottle having a capacity that does not exceed 10 ml, containing enteral feeding material, and having a top end with a threaded section and a bottom end comprising a funneled connector port; and a threaded cap dimensioned to mate with the threaded section of the one-piece bottle; wherein the funneled connector port connects to an enteral feeding assembly; wherein the threaded cap provides a leak proof seal such that there is no exposure point until it is used for feeding, thereby preventing contamination.

Abstract: A flexible container for fluid administration is provided having a body defining a cavity, a base, and at least one port comprising a flange in contact with a flange of a terminal port having a punctureable membrane layer. The body has a cross-sectional configuration including a lower body section of a first dimension, a middle body section of a second dimension, and an upper body section of a third dimension, wherein the second dimension is smaller than the first dimension and the third dimension. The flexible container may also include a base having a plurality of creases that are foldable to form two folded ends each including an extension having a base of a first dimension and a tip of a second dimension.

Abstract: A drug solution filling plastic ampoule having gas, steam and light ray barrier properties, a drug permeation preventing capability and an absorption/adsorption preventing capability, and a production method for the plastic ampoule. The drug solution filling plastic ampoule includes a container body, a fusion-bonded portion which seals a mouth of the container body, and a wrench-off holder tab connected to the fusion-bonded portion. The ampoule is formed from a parison including two or more layers, at least one of which is a functional layer having at least one characteristic property selected from the group consisting of a gas permeation preventing capability, a steam permeation preventing capability, a light ray permeation preventing capability, a drug permeation preventing capability and a drug absorption/adsorption preventing capability.

Abstract: The kit for suppressing drug craving K is used by connecting an instrument for suppressing drug craving 1 to a syringe 2 and the instrument for suppressing drug craving 1 has a cylindrical housing 11, a pouch 12 provided in the housing and containing pseudo-blood B and a connecting member 13 with which the distal end of a syringe is coupled and which cause the syringe to communicate with the interior of the pouch. When the syringe accommodating pseudo-drug M is connected to the instrument and the plunger is moved forward (pseudo-priming), the pseudo-drug M flows into a pouch and the pouch inflates (FIG. 2(b)), and if the plunger 4 is pulled back from this condition, the pouch 12 deflates and the pseudo-blood B flows back from the pouch 12 to the syringe 2 (flashback) (FIG. 2(C)).

Abstract: In one embodiment, a method of filling a container with a liquid drug from a drug reservoir may include: a) connecting a container and a drug reservoir with a cannula such that the drug reservoir and the container fluidically communicate with each other via the cannula, while being hermetically sealed; b) reducing a first volume contained within the container to displace a gaseous medium from the first volume of the container via the cannula into a second volume contained within the drug reservoir; c) increasing the first volume of the container to displace the liquid drug from the second volume of the drug reservoir into the first volume of the container to fill the container; and d) disconnecting the container and the drug reservoir. Before performing action d), action b) and action c) can be successively performed more than once to stepwise increase an amount of liquid drug displaced.

Abstract: The present invention provides a one-piece bottle containing enteral feeding material and having a top end with a threaded section and a bottom end comprising a funneled connector port; and a threaded cap dimensioned to mate with the threaded section of the one-piece bottle; wherein the funneled connector port connects to an enteral feeding assembly; wherein the threaded cap provides a leak proof seal such that there is no exposure point until it is used for feeding, thereby preventing contamination.

Abstract: The present invention relates to a contact protection apparatus for covering a connection point of a medical fluid-conducting cassette for a medical fluid treatment, having at least one covering device for covering the connection point before the use of the cassette, and having at least one connection section for detachably connecting or holding the contact protection apparatus on the cassette. The present invention further relates to a medical fluid-conducting cassette having at least one contact protection apparatus according to the present invention.

Abstract: A container for collecting, transporting, storing, delivering and dispensing fluid. The container has a hollow tube with an outer circumference diameter and is configured to receive a plunger. The container also has a circumferential seal assembly secured at one end of the hollow tube. The seal assembly outer diameter is substantially similar to the hollow tube outer diameter.

Abstract: The calibrated medicine mixing assembly preferably includes a primary reservoir having a primary cavity adapted to receive the fluid. The primary reservoir preferably including calibrated fluid level indicia displayed on an outer surface. Such an assembly may further include a secondary reservoir preferably having a secondary cavity adapted to receive the powder agent. The secondary reservoir preferably including calibrated level indicia displayed on its outer surface. The secondary reservoir is further removably positioned into the primary reservoir such that a major surface area of the secondary reservoir is completely submerged inside the primary reservoir. A plurality of orifices may preferably be formed along a top region of the secondary reservoir, the orifices further situated inside the primary reservoir, thereby causing the secondary cavity to be in fluid communication with the primary cavity when the secondary reservoir is situated within the primary reservoir.

Abstract: Described is a spring-loaded cartridge cap for use in a drug infusion pump. The cap is ejected if it is not properly inserted into the pump. In one embodiment, the cap includes three detent pins that mate with detents in a cartridge chamber within the drug infusion pump. As the cap is inserted into the cartridge chamber of the drug infusion pump, the distal end of the cartridge compresses a coil spring within the cap. To secure the cap within the cartridge chamber, the cap is rotated such that each detent pin moves within a slot until a locking detent is engaged.

Abstract: Anti-vacuum-lock assemblies for preventing vacuum lock when withdrawing medicinal fluid from a vial comprising a multi-finger bung-type stopper in which the fingers are of sufficient length to protect a collapsing or expanding bladder in the vial from being punctured by the hypodermic needle. In a first embodiment the vial includes one or more side or bottom wall holes to permit ambient air to enter in the space between an internal bladder containing a medicinal fluid and the inner wall of the vial. In another embodiment, an expanding bladder in communication with the exterior expands as fluid is withdrawn from the vial. In a third embodiment a fluted collar is inserted in the vial neck to provide air passages into the space between the medicinal fluid-containing bladder and the interior wall of the vial. The collapse of the medicinal bladder or expansion of the compensation bellows or bladder prevents vacuum lock.

Abstract: A multi-medicament container including a vessel body, a plurality of plungers, and a rod is disclosed. The vessel body has an opening end and a closed end. The plungers are received in the vessel body, with the plungers spaced from each other to define a plurality of chambers in the vessel body, with each of the plungers having a passage, and with the passages having a common central line. The rod detachably and fluid-tightly stuffs the passages of the plungers, with an end of the rod extending out of the vessel body from the opening end of the vessel body.

Abstract: A collecting device for fluids for medical use may include a rigid container internally defining a first chamber having a fixed volume, an auxiliary container having a deformable portion defining internally thereof a second chamber having a variable volume as a function of a deformable portion thereof, a passage able to set the first and the second chamber in fluid communication, an inlet port connected to at least one of the containers, and an outlet port connected to at least one of the containers, as well as a bypass line for bypassing the device.

Abstract: An antiseptic applicator device having a reservoir for storing an antiseptic agent, the reservoir being coupled to an applicator pad, and a defeatable membrane being interposed between the reservoir and the applicator pad. Embodiments of the device further include opposing handles, wherein an interior lumen of each handle houses a breakable phial containing a desired solution, and wherein upon moving the handles to a closed position, the phials are broken to release the desired solutions which are then absorbed by the applicator pad.

Abstract: A first connector 2 is provided with: a first connector body composed of a cylindrical outer tube 4, a cylindrical inner tube 7, and a hub 12; a hollow needle 5 supported by the hub 12; a first sealing member supported by the inner tube 7; a coil spring 8 serving as a biasing means which biases the hub 12 in a proximal direction and also serving as a to-be-pierced section biasing means which biases the first sealing member in the distal direction; and gripping and pressing members disposed on the outer tube 4. A plurality of pawls 126 are formed on a flange 124 of the hub 12. A plurality of ratchet teeth 41 are formed on the inner circumferential portion of a proximal portion of the outer tube 4. Each of the ratchet teeth 41 and each of the pawls 126 of the hub 12 form an engagement-disengagement mechanism 13.

Abstract: A container (10) comprising a plurality of compartments (A, B, C) separated by compartment dividers (6), and an inlet connector (3) for receiving a liquid via a connection tube (2). The compartment dividers rupture when a sufficient pressure is applied by a liquid or gas introduced into the container (10) through the inlet connector (3). Some of the compartments comprise powder, which dissolves at the introduction of liquid into the container. A system, process and use in the field of dialysis are also disclosed.

Abstract: A wound closure apparatus and associated methods are provided which utilize blood fluid by activating the clotting cascade of blood fluid within a substantially enclosed sterile container then introducing the blood fluid to the wound site to complete clotting. An apparatus for providing ways of inhibiting anticoagulating agents and slowing fibrin clot degradation are also disclosed. Kits are also disclosed. The invention provides a clotting cascade initiation apparatus including a substantially enclosed sterile containment chamber within which an aliquot of blood fluid, either autologous or from donor sources, can be received and retained. In preferred embodiments, the sterile containment chamber further includes a heparin binding agent which will bind heparin and remove it from the blood fluid. In further embodiments, the containment chamber will also include a procoagulating agent, wherein a clotting cascade can be initiated when the blood fluid is accepted into the sterile containment chamber.

Abstract: A system and method for intermixing the contents of two containers. The system includes a first container, a second container, and a connector for providing fluid communication between the first and second containers. The connector includes at least one resilient retention member for securing the first container to the connector. In addition, the connector accommodates standard vials containing, for example, medicaments, and prevents the unwanted discharge of the contents of the vial into the environment.

Abstract: Disclosed is a system to separate, enrich, and/or purify a cellular population from a biological tissue, such as a tissue sample. For example, an adipose tissue sample can be acquired and disrupted. The disrupted tissue sample can then be separated and purified. The separated components can include multipotent, pluripotent, or other cell populations.

Abstract: The present invention relates to methods, compositions and kits for increasing the in vivo circulation time of isolated platelets by storing the platelets with one or more sialidase inhibitors.

Abstract: This invention relates to medical devices for labelling a syringe filled from an ampoule, and to safer devices for filling a syringe from an ampoule, and to associated methods. We describe a device for attaching to an ampoule to label a syringe filled from the ampoule, the device comprising: an ampoule-mounting portion for mounting the device to a filled ampoule; a syringe-fitting portion to enable the device to be fitted onto said syringe; and a label holder to hold a label for contents of said ampoule; and wherein one of said syringe and said ampoule is detachable from said device; and wherein said label is configured such that in conjunction with a filling operation of said syringe and detachment of said one of said syringe and said ampoule from said device said syringe is labelled by said label.

Abstract: A inert sampling needle is provided for piercing a septum of a vial containing a sample. The sampling needle includes a hollow rigid support member having an inner wall, an outer wall, and a septum-piercing end. The sampling needle also includes a sheath member affixed to the rigid support member. The sheath member covers the septum-piercing end of the support member, the inner wall, and at least a portion of the outer wall adjacent the septum-piercing end to isolate the support member from the sample. Preferably, the sheath member is formed of polyetheretherketone and is affixed to the rigid support member by heat fusing. A method of forming, and a method of using the inert sampling needle is also disclosed.

Abstract: The present invention relates to an apparatus for controlled rate dispensing of a liquid contained in a flexible bag, said apparatus including a chamber adapted to contain the flexible bag containing the liquid, an outlet from the chamber adapted to receive an outlet conduit communicating with the interior of the flexible bag, a source of gas arranged to apply pressure to at least part of the exterior walls of the flexible bag, and a pressure regulator arranged to control the pressure applied to said exterior walls, whereby pressure applied to said exterior walls causes liquid to be dispensed from the flexible bad through the outlet conduit at a controlled rate. A method of delivering liquid at a controlled rate using the apparatus of the present invention is also described.

Abstract: The present invention relates to intravenous (IV) administration apparatus (1) and more particularly to a mobile intravenous (IV) administration apparatus (1) that can be fasten to a human body. The apparatus (1) is having a holder assembly (2) which pivotedly holding IV drip bag (4) such that the IV drip bag (4) may swing freely and maintain in its upright position regardless of the movement of the patient. The top cover of the holder assembly (2) may be raised or lowered to fit different sizes of IV drip bag (4).

Abstract: A sampling device includes a body, a needle, a sealing element and an element for feeding and removing a liquid. The needle has at least one groove located between the sealing element and the sampling end of the needle. The sampling end has a sampling hole opening out on a lateral wall of the end. The sampling device leakage problems encountered in the conventional art to be overcome while at the same time resolving the problems of placing the inside of a tube containing a product to be analyzed at atmospheric pressure.

Abstract: The present invention provides a one-piece bottle containing enteral feeding material and having a top end with a threaded section and a bottom end comprising a funneled connector port; and a threaded cap dimensioned to mate with the threaded section of the one-piece bottle; wherein the funneled connector port connects to an enteral feeding assembly; wherein the threaded cap provides a leak proof seal when tightened on the threaded section of the one-piece bottle, and allows venting of the bottle when loosened.

Abstract: A system for transferring solutions from a first cartridge into a second cartridge comprises a cartridge holder, a plunger driver, and a cartridge connector. The cartridge connector carries a transfer needle and an exhaust needle. The cartridge holder positions the first cartridge against the cartridge connector so that the transfer needle penetrates the first cartridge septum. The second cartridge is removably inserted into another end of the cartridge connector so that both the transfer needle and the exhaust needle penetrate the second cartridge septum. The plunger driver is disposed to advance a plunger on the first cartridge to transfer solution from the first cartridge into the second cartridge thus displacing solution from the second cartridge through the exhaust needle. The cartridge connector includes a sealed interior waste chamber for receiving the solution from the second cartridge.

Abstract: A female piercing member protection device for connection with a male connection part, and a method for connecting the device to a male connection part. The device includes an outer casing and a connection member at least partly enclosed in the outer casing. The outer casing is moveable between first and second positions. In the first position, the connection member is substantially locked from movement along the longitudinal axis A, and in the second position the connection member is able to move along the longitudinal axis A. The device also has an activated position and an inactivated position. When the outer casing is in the second position, a deformable locking device is prevented from deformation by the outer casing to prevent disengagement of the male connection part. A secure piercing member protection device significantly minimizes the risk for a user to be exposed to contaminants and the piercing member itself.

Abstract: Embodiments of the present disclosure provide a medical product with a biodegradable portion. The biodegradable portion is made of a biodegradable material and the biodegradable portion degrades faster than the remaining portion of the medical product.