Abstract: A flexible non-PVC, non-DEHP polyolefin container or bag for medical fluids has an elongated container body formed of polyolefin film. The container has one or more ports equipped with a polyolefin fill tube and port closure assembly. The container includes a concave seam on at least one of its longitudinal sides.

Abstract: A method used in connection with processing of blood components, wherein blood products are then filtered via a filter rotating along with a centrifuge rotor and the sensed pressure may be used in connection with controlling the pumping of the blood products and/or in connection with determining the location of an interface associated with the blood products.

Abstract: A holder for receiving a sampling tube of a blood sampling system is disclosed. The holder has an interior pocket which can be conformed from a closed position to an open position for receiving the sampling tube.

Abstract: Provided a port member for an infusion solution bag that is capable of suppressing occurrence of gaps or wrinkles in a sealed portion in a manufacturing process, and preventing damages to resin sheets of a bag body during storage or transportation. A port member for an infusion solution bag includes a tubular body portion having one end sealed by a plug member structured to enable a hollow needle to be pierced into the plug member, and a tubular to-be-sealed portion continuously formed with an other end of the body portion and having an inner space communicated with the inside of the body portion, the to-be-sealed portion being held between and sealed to end portions of resin sheets overlapped together to form a bag body having an inner space for accommodation of at least a medicine, in which the to-be-sealed portion thus sealed has a radially flattened shape.

Abstract: A hydrogenated norbornene ring-open polymer obtained by hydrogenating 80% or more of main-chain carbon-carbon double bonds of a ring-open polymer which is obtained by ring-opening polymerization of 2-norbornene is disclosed. The hydrogenated norbornene ring-open polymer has a weight average molecular weight (Mw) determined by gel permeation chromatography (GPC) of 50,000 to 200,000, a molecular weight distribution (Mw/Mn) of 1.5 to 10.0, and a melting point of 110 to 145° C.

Abstract: A collapsible fluid containment bag for irrigating and cleaning wounds on extremities having semi-rigid support members and an elevated lower support member attached to the bottom of the proximal end of the containment bag creating a gradient for allowing irrigation fluids and biological tissue to drain to the distal end of the bag for removal. The containment bag is collapsible, making it a convenient size for storage, transport, and disposal.

Abstract: The invention includes a bag system for collecting a biological fluid, in particular blood. The system includes a device for collecting the fluid which is in fluid communication with at least one fluid collection bag, and a device for sampling the fluid to be collected which includes at least one sampling receptacle. The sampling device includes a device for transferring the fluid from the bag system into the sampling receptacle or receptacles, in which the transfer device is provided with a device for associating the receptacle or receptacles. The transfer device may be arranged to allow the support of the receptacle or receptacles in a standby position, the guidance of the receptacle or receptacles to a transfer position and, after transfer, the dissociation of the receptacle or receptacles from the bag system.

Abstract: The invention relates to a method for priming a blood tubing set comprising a venous and an arterial line whose connections at the patient side are in communication with two separate inlets of a chamber of in particular a bag and whose connections at the machine side are in communication with a dialyzer comprising the steps: parallel filling of both the venous and the arterial line via a feed line so that priming liquid flows through both inlets into the chamber; and circulation of the priming liquid in the circuit of the lines, the dialyzer and the chamber via a pump so that one of the inlets of the chamber acts as an inlet and the other as an outlet. The invention likewise comprises a corresponding blood tubing set and a bag as well as methods for providing them.

Abstract: A medical fluid container of a flexible plastic material is produced as follows: at first, a plastic compound is produced from a heterogeneous mixture of a first, lower-viscosity raw polymer component having a first melt viscosity and a second, higher-viscosity raw polymer component having a second melt viscosity which is greater than the first melt viscosity. Then the plastic compound is extruded. The extrudate is confectioned. Finally, the confectioned extrudate is sealed to form the finished fluid container. A film tubing may serve as intermediate product for the medical container. The medical container or the film tubing thus produced has surface structures with a typical average size of 15 to 200 ?m. The production method requires little effort while fulfilling demanding requirements with respect to the stability of the produced fluid container.

Abstract: Multi-layered film consisting of at least an inner layer (3) and an outer layer (2), with an intermediate layer (4) provided in between, whereby at least the inner and the outer layers (2-3) consist of a homopolymer of polypropylene and/or a copolymer of polypropylene, and whereby the intermediate layer (4) contains at least a mixture of a homopolymer of polypropylene and/or a copolymer of polypropylene with a thermoplastic elastomer, characterized in that the film (1) has a haze of 5% or less.

Abstract: The invention relates to the field of containers for providing liquid dialysate concentrates for a dialysis treatment of a patient with the aid of an artificial kidney. Up to now such concentrates have been delivered mainly in rigid plastic containers as the weight of the concentrate requires a certain stability of the container. Such containers also simplify the shipping of large loads as they can easily be arranged in layers on top of each other. These rigid containers have the disadvantage that because of their rigidity they are comparatively expensive as the container walls have to be thick enough leading to higher material expenses. Furthermore, the empty containers are bulky making the further processing cumbersome. The large amount of material to be recycled or discarded adds further to the cost. The invention avoids these drawbacks by proposing a container filled with a liquid dialysate concentrate that is a self-standing bag (1) made of flexible elastomeric sheets.

Abstract: The invention relates to a bag system for the cryopreservation of body fluids, that is blood, bone marrow or umbilical cord blood, the parts of the bag system being sterilized, and separable from one another, wherein liquids which permit and/or assist cryopreservation are located in the bag system and/or may be introduced into the bag system in a sterile form. The bag system, at least, comprising: a device for the direct removal of body fluid (1) from the living body, a region or number of regions for mixing the liquids with the body fluid and/or for storing the mixture of liquids and body fluid, a number of shut-off elements (2) and connecting lines (3) and an inlet element (4) and/or an outlet element (5).

Abstract: A flexible container incorporating flexible front and rear sheets and one or more container ports disposed in between the sheets are discussed. The one or more container ports each has a pliable attachment flange and an integrally molded nozzle. The pliable attachment flange has a first configuration whereby the attachment flange collapses to enable heat sealing the attachment flange to the sheets and thereafter substantially recovers its shape to provide a fluid pathway with the port. Various terminal ports, terminal caps, and rubber septums may be useable with the one or more container ports.

Abstract: A multiple chamber medical fluid bag including: (i) a flexible enclosure; (ii) a first fluid chamber formed in the enclosure; (iii) a second fluid chamber formed in the enclosure; (iv) the first fluid chamber and the second fluid chamber separated by a frangible seal; and (v) an access port connected to the enclosure, the enclosure folded so as to cover the access port and so that the frangible seal is broken to uncover the access port.

Abstract: A needleless access port is assembled from parts sealed to a flexible container, such as a container for intravenous infusion, parenteral nutrition or transfusion. The port includes a lower housing for sealing to the container, the lower housing having an upright tower for mounting an upper housing. The upper housing has at least one connector or valve and a sleeve for mounting to the tower. The sleeve includes connectors so the upper housing can be mounted in a first, upper resting position, and a second lower, active position, for adding liquid to the container or for removing liquid from the container. Even after assembly to a container, the upper housing may be removed and the lower housing may be used instead with a standard IV spike set.

Abstract: A rigid double-port tube with medicine dispensing nozzle for the big transfusion soft bag, which consists of a rigid double-port (1) and a medicine dispensing nozzle (2) through which the medicine is dispensed, through the rigid double-port (1) the medicine is infused into the soft bag and the medicine liquid is exported from the soft bag; the rigid double-port (1) consists of a medicine infusing port (11), a medicine dispensing port (12) disposed parallel to the medicine infusing port (11), and the connecting base (13) connecting the medicine infusing port (11) and the medicine dispensing port (12), the medicine dispensing port (12) is connected with the medicine dispensing nozzle (2) hermetically; a sealing rubber plug (22) used to medicine dispensing is disposed onto the medicine dispensing nozzle (2), the sealing rubber plug (22) can be pierced by the syringe pinhead and it contracts and closes automatically after the syringe pinhead being pulled out.

Abstract: The invention is directed to a system for continuously filtering a blood product including whole blood or any of its component(s), erythrocytes, leukocytes, platelets and plasma either alone or in combination. The system includes a connector for receiving the blood product, a filter coupled to the connector for filtering the received blood product, a collection bag coupled to the filter for collecting the filtered blood product, and a reservoir bag connected to the connector for temporarily storing received blood product, and providing received blood product through the connector to the filter to maintain continuity in filtration. The reservoir bag and the collection bag are suspended, the connector near or below the bottom of the collection bag, and the bottom of the reservoir bag is above the bottom of the collection bag. Also provided is a method of filtering a blood product using the continuous blood filtration system.

Abstract: A liquid storage bag having a partition wall allowed to be peeled easily and not peeled by an accidental drop, etc. The liquid storage bag is one wherein the upper part thereof is closed with a freely and closable zipper, the bottom thereof is provided with a liquid outlet, and an easily peelable partition wall (a weak seal part) is provided close to the zipper. The internal space of the liquid storage bag is divided liquid-tightly into upper and lower parts through this weak seal part, liquid is stored in the lower part of the internal space (liquid storage chamber), and the weak seal part is formed in outside-convex form at a center and increased in width at both end parts thereof.

Abstract: A reservoir for a nebulizer, a nebulizer and a method of filling a reservoir are proposed. To avoid undesirable rises in pressure, a fluid chamber of the reservoir is pre-collapsed and filled with an initial amount of fluid which is less than the maximum volume of the fluid chamber. Preferably, before being filled, the fluid chamber is compressed and/or expanded by means of gas to a defined volume which is less than the maximum volume of the fluid chamber.

Abstract: A pouch for mixing and dispensing a composition including a pouch body and a port body. The pouch body includes opposing, first and second major flexible walls sealed to one another along respective peripheries thereof to define an internal chamber and a pouch perimeter. The pouch body has a C-like shape. The port body projects from the first wall and is fluidly open to the internal chamber. With this configuration, various components, such as a powder component and a liquid component, can be mixed by a user's hand(s) in pressing the walls in a kneading fashion, with the resultant composition being dispensed through the port body. In some embodiments, the pouch is provided to a user with a powder component pre-loaded in the internal chamber.

Abstract: A blood collection device includes a collection container, a flexible conduit permanently affixed at a proximal end to the collection container, and a needle permanently affixed to a distal end of the flexible conduit. The collection container, flexible conduit and needle can be provided within a package. A method for collecting blood products is also disclosed.

Abstract: A bag connection comprises a first bag, a tube having a blood-drawing needle at the front end, a plurality of second bags, tubes for connecting the first and second bags, and tubes and branch connectors for connecting the second bags to each other. On the other hand, a filter unit includes a filter, and a tube connected at opposite ends thereof to the inlet and outlet of the filter. The tubes of the bag concatenation and the tube of the filter unit have respective markers attached thereto. With these markers used as marks, both tubes are aseptically connected by a tube aseptic connection device, thereby incorporating the filter unit into an intermediate portion of a tube of the bag concatenation.

Abstract: A culture chamber for use in a method of culturing microbiological material, which comprises a wall or at least a portion of a wall consisting of a gas-permeable membrane, a textured interior growth surface arranged for contact with the microbiological material being cultured and at least a portion of the external surface gas-permeable membrane being textured to enhance gas permeability. Preferably, the gas-permeable membrane is textured over the majority of both of its surfaces. This culture chamber provides enhanced gaseous exchange between the interior and exterior of the culture chamber and increased surface area within the culture chamber for cell attachment.

Abstract: A blood chamber for extracorporeal blood circuits comprises a container body (2) made in a single piece by blowing of a plastic material, and has a plurality of connection ports (3, 4) for fluid communication with outside; each connection port (3, 4) comprises a tubular mouth (6) having a truncoconical internal surface (61) which is coupled in a fluid-proof coupling to a tubular first part (101) of an insert (10), made by injection molding of a plastic material. The insert (10) has a truncoconical and smooth internal surface (102) which is coupled by gluing with a solvent to an end zone of a fluid transport tube (7, 8). The coupling between the blood chamber and the fluid transport tubes is very strong and reliable. The blood chamber is part of an extracorporeal blood circuit which is operatively associated to a dialysis machine.

Abstract: A formed, filled, and sealed container, access port and method for establishing fluid flow from the container to an administrative set is provided. The container is collapsible and has an inlet and an outlet. A hollow port is sealed to the container and a perforator inside the port pierces and becomes embedded in the container. Solution in the container is withdrawn into the port. A line attached to the port and an administrative set further establishes flow between the container and the administration set. The port may be operated with a single-hand to establish fluid flow from the container to the administrative set. After the perforator is embedded in the container, a lock on the port prevents the perforator from removal from the container. Activation of the lock produces an audible and/or visible notification.

Abstract: A communicating member for a medical container contains a plate member 4 having a first opening 5 and a second opening 6, a first connection port 15 including the first opening 5, a plug 9 that obturates the first opening 5 and a first approximately cylindrical member 19 that is in communication with the first opening 5, a second connection port 16 including the second opening 6 and a barrier member 13 that obturates the second opening 6, and a continuous wall 17 disposed on the plate member 4 on the first approximately cylindrical member 19 side and disposed upright on the plate member 4 such that the continuous wall 17 encloses the first opening 5 and the second opening 6 when the plate member is viewed from above; and the first approximately cylindrical member 19 is provided with a first communication part 20 that has an opening on the second opening 6 side.

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 system and method for autologous normovolemic hemodilution (ANH) are disclosed. The system can include a vacuum canister, which is sized to accept donor bags of a predetermined capacity. The vacuum canister is connected to a vacuum source which applies a suction to the donor bag within the canister. The system can include a canister having a self-generated vacuum, which includes compressible sidewalls that are spring-loaded to provide negative pressure needed to collect blood from a patient without the use of a gravity-induced siphon gradient. Also disclosed are ANH systems and kits that rely on a gravity-induced siphon gradient for blood collection.

Abstract: A system for automatically processing blood components is described. The system includes a console, which contains all motors, pumps, sensors, valves and control circuitry, and a unique disposable set that includes a cassette supporting a centrifuge with an improved design, pump interfaces with an improved design, component and solution bags, and tubing. Various processes are implemented using a specific disposable set for each process which allows automatic identification of the process to be performed the console.

Abstract: A flexible non-PVC, non-DEHP container or bag for medical fluids has a container body formed of a multiple layer polyolefin film. The container has one or more ports equipped with a polyolefin fill tube and port closure assembly. The container has a low moisture vapor transmission rate.

Abstract: A head part (11) for a multi-chamber tube bag (1) with a multi-component mass which can be pressed out, having a main chamber (2) for a first component and two secondary chambers (3, 4) for two other components, has a disk-shaped contact surface (12) for the multi-chamber tube bag (1) surrounding a press-out opening (13). At the contact surface (12), a plurality of raised portions (14) project toward the multi-chamber tube bag (1) and are provided at the head part (11) for narrowing the outlet regions (5, 6) of the two secondary chambers (3, 4) of the multi-chamber tube bag (1) when the multi-chamber tube bag (1) bears against the contact surface (12).

Abstract: A system and method are used in connection with processing of blood components. The processing of blood components may involve centrifugal separation and/or filtering of the blood components. In some examples, at least some blood components are centrifugally separated in a chamber and then filtered via a filter rotating along with a centrifuge rotor, wherein the filter is located closer than the chamber to an axis of rotation of the rotor. The filter may include a porous filtration medium configured to filter leukocytes, platelets, and/or red blood cells. Some examples include a pressure sensor sensing pressure of pumped blood components. The sensed pressure may be used in connection with controlling the pumping of the blood products and/or in connection with determining the location of an interface associated with the blood products. Other uses of the sensed pressure are also possible.

Abstract: A multilayer plastic container for storing lyophilized products includes at least three layers consisting of inner and outer layers having a moisture vapor transmission rate of not more than 0.1 gm mil/100 sq. in.—day at 73° F. and 95% rh, and an intermediate layer of hygroscopic resin construction having a moisture content less than 1000 ppm. The hygroscopic intermediate layer preferably comprises at least 30% of the total thickness of the three layers. The inner and outer layers preferably are of cyclic olefin polymer or cyclic olefin copolymer construction, and the hygroscopic intermediate layer preferably is of amorphous nylon construction. The container preferably is empty and sealed within a secondary container, such as a metallized bag, that is impervious to moisture.

Abstract: The present invention provides a fluid reservoir comprising a first wall portion formed from a needle-penetrable material, the first wall portion comprising a seal surface. The reservoir further comprises a seal member formed from a needle-penetratable self-sealing material, wherein the seal member has been applied on the seal surface in a liquid state. In this way a liquid reservoir having a self-sealing needle-penetrable access means which can be manufactured in a cost-effective manner is provided.

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: An infusion bag according to one exemplary embodiment includes a body having an interior space for holding a fluid. The interior space is defined by a pair of side walls and an inner wall and an opposite bottom wall. The inner wall extends across the body from one side wall to the other side wall such that a first angle ?1 is formed between a first end of the inner wall and one side wall and a second angle ?2 is formed between a second end of the inner wall and the other side wall. The first angle is different from the second angle. The bag also includes a needleless port that is in fluid communication with the interior and is configured to sealingly mate with an external device. The needless port is disposed in an upper corner of the body where the second end of the inner wall intersects the other side wall.

Abstract: A sampling apparatus is disclosed that includes a sample container including at least one wall defining a fluid-receiving interior chamber and including a fluid inlet for receiving fluid into the chamber and a sample device receiver carried by the container wall and in fluid communication with the chamber, the receiver being adapted to receive a sampling device for withdrawing a fluid sample from the chamber.

Abstract: Safety apparatus for transfusions of blood or blood derivatives contained inside at least one bag (1) having at the bottom at least one tube (2) made of elastically deformable material such as rubber or the like, for discharging the blood or blood derivatives; said blood or blood derivatives belong to a given blood group with an associated Rh factor; said apparatus comprises a constriction device (3) closed by suitable clamping means (14, 15) movable about said tube (2) so as to prevent the blood or blood derivatives which leave the bag (1) from passing through said tube (2); said constriction device (3) is provided with a seat (4) on which suitable elements (6,7) for coding and identifying said blood group with associated Rh factor are formed, which elements co-operate with a unique key (19) which establishes the identity of the blood group of the patient and, in the event of compatibility, allows opening of said constriction device (3) provided with suitable elements (5, 21, 22) complementing said coding el

Abstract: A medicant reconstitution system is provided which has a generally flexible fluid bag with associated administration and reconstitution ports. The reconstitution port is adapted for receiving a medicant container and the administration port is for administering a medical fluid to a patient. According to one aspect of the present invention, the administration and reconstitution ports are integrated in a relatively rigid port structure. According to another aspect of the present invention, the reconstitution port receives a piercing member which is rotatable to a selected position to establish fluid flow. According to yet another aspect of the present invention, one of the reconstitution port and the piercing member includes a cutting edge, while the other includes a frangible member. Contact between the cutting edge and the frangible member opens the frangible member to establish fluid flow.

Abstract: A disposable fluid circuit kit for extracorporeal blood treatment systems that supply replacement fluid to a patient is described. The circuit has a blood portion that carries blood and subjects it to some treatment, such as dialysis or hemofiltration. A portion carries filtrate or dialysate. A replacement fluid portion that carries fluid used to compensate for fluid loss is connectable to a supply of replacement fluid. a sterilizing filter in the replacement fluid portion sterilizes the replacement fluid before introduction into the patient acting as a guard against touch contamination of the connected replacement fluid container. Preferably, the filter has a pore size effective to eliminate pyrogens.

Abstract: A portable, hands-free and user friendly breast pump for facilitating breast-feeding, incorporates a dome-shaped housing having a servomotor mechanism; a hat-shaped flange having a chamber portion, a brim portion and an outlet, the chamber portion being formed so as to be placed over a nipple on a breast so as to define a chamber between the flange and the breast, and the brim portion being formed to surround the nipple and thereby form a suction seal therebetween; and a one-way venting element formed to operatively communicate with the chamber so as to vent pumped milk from the chamber via the outlet. The housing, the flange and the venting element are connected into an integral device held against the breast and underneath clothing so as to keep the integral device hidden. Breast milk is collected via a plastic collection bag that connects directly with the pump underneath clothing such that the milk is isolated from any contaminants in the air and may be easily stored immediately after being collected.

Abstract: An IV product comprises a flexible fluid bag and a container housing for supporting and protecting the fluid bag. The IV product may include an information element such as a bar code, RFID or the like which provides information. The IV product may also include a mechanism for expelling fluid from the fluid bag, such as an inflatable bellows. In one embodiment, the IV product may be mated to a docking station or receptacle. One or more elements may be provided for aligning and connecting the IV product to establish a fluid connection with the fluid bag.

Abstract: Stable single bicarbonate-based solutions are provided. The bicarbonate-based single solution of the present invention includes at least calcium and bicarbonate and is stored or packaged in a sterile manner within a container with a gas barrier. The single solutions of the present invention can remain stable for three months or more. In this regard, the stable and single bicarbonate-based solutions of the present invention can be readily and effectively used during medical therapy, such as dialysis therapy.

Abstract: A hemoglobin solution packaged in a flexible oxygen-impermeable container system. The container system includes a multi-layer film having at least a product contact layer, an oxygen and moisture barrier layer and an exterior layer. The flexible container system further includes an interface port for filling the flexible container with the hemoglobin solution and delivering the hemoglobin solution. The hemoglobin solution comprises a substantially stroma and tetramer free, cross linked, pyridoxylated hemoglobin solution including preservatives such as ascorbic acid, glycine and dextrose.

Abstract: Improvements in a mini-osmotic pump and coating compositions are described. The dispensing pump includes an inner fluid-filled bag encased by an osmotic layer and outer, semi-permeable membrane. The inner bag is formed with an arcuate edge at the open end of the bag to inhibit formation of fissures in the outer membrane in this edge region. The coating compositions include cellulose acetate butyrate, cellulose acetate propionate, and polymethylmethacrylate polymers, optionally mixed with ethyl cellulose in acetone based solvent systems.

Abstract: A device (2) for a body fluid bag, includes a filtering part (5) and a retransfusion part (6), the filtering part (5) having a filtering part inlet opening (7) and a filtering part outlet opening (8). The outlet opening (8) is arranged to be connected to an inlet opening of the body fluid bag, and the retransfusion part (6) has a retransfusion part inlet opening (10), being arranged to be connected to an outlet opening of the body fluid bag, and a retransfusion part outlet opening (11), wherein the filtering part (5) and said retransfusion part (6) are mechanically integrated to form a single unit. A transfusion unit (16) including such a device (2) is also disclosed.

Abstract: An extraction device for a biological fluid with an additive solution in which it is desirable for the additive solution to be present in a particular volume proportion to the biological fluid. The volume proportion of the additive solution is determined by the ratio of cross sections of two tubes, one which supplies the biological fluid to a collecting bag and a second which supplies the additive solution to a collecting bag. The tubes are periodically constricted in constriction areas by a pump. The tubes are configured so that the additive solution and the biological fluid only mix downstream of the constriction areas, thereby reducing the risk of supplying the additive solution to the source of the biological fluid. In an exemplary embodiment the biological fluid is blood collected from a patient or donor and the additive solution is an anticoagulant and/or preservation solution.

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: Disclosed is an infusion pump and a fluid container for expelling a fluid from the fluid container to a patient. The pump comprises a housing having a chamber therein for receiving the fluid reservoir. A first wall is provided on the housing for contacting the fluid reservoir, and a second wall is movable from a first position distanced from the first wall to form the chamber therebetween, and a second position relatively closer to the first wall. Advancing the movable wall from the first position to the second position expels fluid from the collapsible reservoir. Preferably, the first and second walls are provided with non-planar complementary surface configurations for contacting the collapsible reservoir. Retraction mechanisms for retracting the movable wall from the second position to the first position, and user readable indicium of the status of the dispensation cycle are also disclosed.

Abstract: The present invention provides an improved kit for the collection of umbilical cord blood and placental blood, and collection of the placenta from which such blood is obtained. The kit improves upon existing kits in that it provides for improved user convenience, provides for the collection of the placenta itself, and better maintains the internal temperature of the container in which the collected blood and placenta are shipped to a blood bank or registry. The invention further provides a method of collecting umbilical cord and placental blood, and the placenta from which such blood is obtained, comprising using the kit described herein.