Abstract: Disclosed is a dispenser having a first chamber containing a first fluid and a second chamber containing a second material. Each chamber has screw threads that are selectively joinable so that the first and second chambers are twistable relative to one another. The first chamber includes an open top end that is, before use, covered with a breakable membrane. A breaker ring is located within the second chamber and is configured to break the breakable membrane when the dispenser is transitioned between an extended position and a compact position. In the compact position with the breakable membrane broken, the first fluid and second material form a mixture that can be dispensed via an opening in an openable tip.

Abstract: The double packing materials according to the present invention which primarily packs the infusion solution with a polypropylene packing material and secondarily vacuum packs and hermetically seals the packed polyethylene packing material with a material including an aluminum foil ensures safety of the content therein from light and has high thermal resistance and excellent preservation properties that resists to the damage and tearing by external force on long-term storage despite that it is not stored in dark place, and thus is very useful as the packing material for storing expensive infusion solution such as the contrast medium which is radiological diagnostic solution.

Abstract: A container is provided comprising a body defined, at least in part, by a film, the body including at least one side seal, at least two chambers separated, at least in part, by a peelable seal, and the film including a sealant layer having a bimodal thermal behavior such that the side seal is a permanent seal and the peelable seal can, at least in part, be separated.

Abstract: An apparatus and method for collecting whole blood and then separating it into components for subsequent use or storage. A self-contained bag set is used to collect the sample, which may then be placed into a device adapted to fit into a centrifuge for separation of components. Each component is then sequentially extracted according to density, with a sensor present in the device to control the operation of valves directing the collection of each component. The sensor may be reading one or more of the following characteristics: infrared, optics, density, weight, radioactive, fluorescence, color, magnetism, ultrasonic, capacitance wherein the characteristic is inherent in the blood and blood component or is an additive. Each component may then be separated into its own storage container. The preferred sensors include optics and weight.

Abstract: The invention provides container systems, kits and methods for peritoneal dialysis (PD) solutions. Such a system, for example, includes a first compartment that contains a PD osmotic agent and a second compartment that contains a PD buffer agent. The compartments maintain their respective contents separately from one another for purposes of transport, storage and/or sterilization. However, the compartments are fluidly couplable, so that their respective contents can be combined with one another, e.g., following sterilization of the agents and prior to their introduction into the patient's abdomen. The invention provides, in other aspects, such systems, kits and methods that provide protective structure which inhibits breaking of a seal prior between the second compartment and an outlet of the system, prior to breaking of a seal between the first and second compartments.

Abstract: The present invention provides modified platelets having a reduced platelet clearance and methods for reducing platelet clearance. Also provided are compositions for the preservation of platelets. The invention also provides methods for making a pharmaceutical composition containing the modified platelets and for administering the pharmaceutical composition to a mammal to mediate hemostasis.

Abstract: A port closure system for use with a fluid container having fluid ports includes administrative and additive port closure assemblies. The administrative assembly receives a piercing pin and includes an administrative housing which seals closed one fluid port. A sleeve extends from an interior surface past a base surface in the administrative housing. The sleeve has an upper portion and a lower portion, of differing diameters. A cap assembly mates with the administrative housing, sealing the interior surface of the administrative housing. A removable cap provides access to the interior surface. The additive assembly receives a needle and includes a reseal housing which seals closed another fluid port. Another cap assembly mates with the reseal housing, sealing an interior face of the reseal housing. Another removable cap provides access to the interior face. A reseal element is mechanically retained between the reseal housing and cap assembly.

Abstract: A port closure system for use with a fluid container having fluid ports includes administrative and additive port closure assemblies. The administrative assembly receives a piercing pin and includes an administrative housing which seals closed one fluid port. A sleeve extends from an interior surface past a base surface in the administrative housing. The sleeve has an upper portion and a lower portion, of differing diameters. A cap assembly mates with the administrative housing, sealing the interior surface of the administrative housing. A removable cap provides access to the interior surface. The additive assembly receives a needle and includes a reseal housing which seals closed another fluid port. Another cap assembly mates with the reseal housing, sealing an interior face of the reseal housing. Another removable cap provides access to the interior face. A reseal element is mechanically retained between the reseal housing and cap assembly.

Abstract: A blood bag system includes a BC pooling bag for centrifugation of a buffy coat, a filter for removing white blood cells from a supernatant liquid transferred from the BC pooling bag, a platelet preserving bag for reserving the supernatant liquid that has passed through the filter, a first tube connecting the BC pooling bag and an inlet of the filter, a second tube connecting the platelet preserving bag and an outlet of the filter, and a cassette to be fixed in the centrifugation and separation apparatus. The first tube and the second tube are disposed within the cassette. The cassette includes a first clamp section for closing and opening the first tube, and a second clamp section for closing and opening the second tube.

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 means for supplying 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 thus transferred blood component is contained.

Abstract: In a blood bag system mounted in a centrifugation and separation apparatus, a filter is settable in different appropriate orientations at storage time and usage time, and first and second tubes and a filter are arranged respectively in appropriate orientations during use. The blood bag system includes a BC pooling bag for centrifugation of buffy coat, the filter for removing white blood cells from a supernatant liquid transferred from the BC pooling bag, a platelet preserving bag for reserving the supernatant liquid that has passed through the filter, the first tube connecting the BC pooling bag and an inlet of the filter, the second tube connecting the platelet preserving bag and an outlet of the filter, a cassette fixable in the centrifugation and separation apparatus, an attachment for holding the filter, and a hinge section tiltable relative to the cassette with reference to an axis in the circumferential direction.

Abstract: The invention provides container systems, kits and methods for peritoneal dialysis (PD) solutions. Such a system, for example, includes a first compartment that contains a PD osmotic agent and a second compartment that contains a PD buffer agent. The compartments maintain their respective contents separately from one another for purposes of transport, storage and/or sterilization. However, the compartments are fluidly couplable, so that their respective contents can be combined with one another, e.g., following sterilization of the agents and prior to their introduction into the patient's abdomen. The invention provides, in other aspects, such systems, kits and methods that provide protective structure which inhibits breaking of a seal prior between the second compartment and an outlet of the system, prior to breaking of a seal between the first and second compartments.

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: An object of the present device is to provide a cover capable of preventing the administration of unmixed medicaments to a patient. The cover for being mounted on a multi-compartment infusion bag of the present device is a cover for being mounted on a multi-compartment infusion bag including a plurality of compartments partitioned by at least one easily peelable partitioning seal portion which is opened in response to an increase in the internal pressure of at least one of the plurality of compartments induced by pressing said at least one of the plurality of compartments. The cover has a pair of pinch members that pinch at least one of the plurality compartments. The pair of pinch members has engaging elements that engage each other to maintain a pinching state of the pair of pinch members until the pinching state is released in response to an increase in the internal pressure of said at least one of the compartments so that the suspension portion can be used.

Abstract: The invention relates to a medical bag which is intended for the infusion of a medicament by means of gravity. The inventive bag comprises: at least two compartments, namely a first compartment (1) containing a medicament in the form of a solution and a second compartment (2) containing a rinsing solution; and means for separating/communicating the compartments, which prevent the rinsing solution from automatically entering the medicament compartment except at the end of the infusion period. The rinsing solution ends the infusion, by rinsing the medicament bag and the infusion line, such as to prevent any risk of contamination or leakage of residual medicament from the bag or line.

Abstract: The invention provides container systems, kits and methods for peritoneal dialysis (PD) solutions. Such a system, for example, includes a first compartment that contains a PD osmotic agent and a second compartment that contains a PD buffer agent. The compartments maintain their respective contents separately from one another for purposes of transport, storage and/or sterilization. However, the compartments are fluidly couplable, so that their respective contents can be combined with one another, e.g., following sterilization of the agents and prior to their introduction into the patient's abdomen.

Abstract: The present invention relates to a multi-chamber medical bag, which is capable of obtaining a positive mixture of medicines, prior to the discharge thereof. A weak seal 24 is provided for dividing the space inside the medical bag 10 into the left-handed and right-handed partitions 26-1 and 26-2. The weak seal 24 has a first portion 24-1 extending between the partitions 26-1 and 26-2 and a bifurcated adjacent to and faced with an outlet port 12. Additional strong seals 30-1 and 30-2 are arranged on both sides of the second portion 24-2 and extend at right angle to the first portion 241 toward the strong seal 14 at the outer periphery of the medical bag. When the partition 26-1 or 26-2 is pressed, the resultant inflated deformation of the medical bag is mainly directed to the first portion 24-1 due to the existence of the additional strong seals 30-1 and 30-2, which allows the last portion to be separated, resulting in a mixing of the medicines in the partitions 26-1 and 26-2.

Abstract: The present invention is directed towards a method and apparatus for packaging or containing, handling and managing of a variety of materials or other contents from a variety of sources which encounter use under various dynamic applications, conditions and for a plurality of purposes. The invention more specifically is directed towards one or more containers or packages, suitably fitted or used for the handling or managing of materials or other contents along one or more cycles or chains of use.

Abstract: Apparatus for reducing the fat content of blood and in particular to an apparatus for reducing the fat content of pericardial suction blood has a conduit for blood, an absorbing filter located in the conduit and an associated temperature control device for adjusting the temperature of blood before it flows through the filter.

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.

Abstract: The present invention provides an enteral feeding set comprising tubing adapted for fluid flow therethrough and further adapted to be engaged by a pump unit, a valve mechanism in direct communication with said tubing, said valve mechanism being adapted to be engaged by said pump unit, and a feeding set indicator for permitting identification of the functional configuration of said administration feeding set by said pump unit, characterized in that said tubing comprises at least two inlet tubes on an upstream side of said valve mechanism and a single outlet tube on a downstream side thereof and wherein said inlet tubes each include a connector for connecting said tube to a supply of fluid at a connection end thereof, each of said connectors being of like form but visually distinguishable for indicating to a user which supply of fluid each connector should be attached thereto.

Abstract: A multi-chamber chemical delivery container for storing dry chemicals that are used to produce a liquid microbial deactivation fluid. The container includes two housing sections and a dividing wall that is located between the two housing sections. The dividing wall separates the container into two compartments. Openings formed in each of the two housing sections are dimensioned to respectively receive an inlet fitting and an outlet fitting. The inlet and outlet fittings are dimensioned to respectively engage with inlet and outlet connectors that are fluidly connected with a fluid circulation system of a microbial deactivation system.

Abstract: In certain embodiments, a vial adaptor for removing liquid contents from a vial includes a piercing member and a bag. The bag can be contained within the piercing member such that the bag is introduced to the vial when the vial adaptor is coupled with the vial. In some embodiments, the bag expands within the vial as liquid is removed from the vial via the adaptor, thereby regulating pressure within the vial. In other embodiments, a vial includes a bag for regulating pressure within the vial as liquid is removed therefrom. In some embodiments, a vial adaptor is coupled with the vial in order to remove the liquid. In some embodiments, as the liquid is removed from the vial via the adaptor, the bag expands within the vial, and in other embodiments, the bag contracts within the vial.

Abstract: A fluid ducting assembly for enabling flow communication between a syringe and either one of a vessel and a dispenser for dispensing a fluid contained, a priori in the syringe or in the vessel. The fluid ducting assembly includes a base having a first member, a second member, and a third member for connection to and providing flow communication with the syringe, the vessel and the dispenser, respectively. The fluid ducting assembly further includes a flow controller within the base enabling any one of a flow path between the first member and the second member and a flow path between the first member and the third member. The flow controller has either a first operative position in which the flow path between the first member and the second member in enabled or a second operative position in which the flow path between the first member and the third member is enabled.

Abstract: There is provided a multi-chamber bag that is capable of securely checking a medicinal substance accommodated therein without the necessity to perform a troublesome work, while preventing a matter deteriorating the medicinal substance from reaching the inside of a medicinal-substance accommodation chamber and hence securely preventing the deterioration of the medicinal substance. In a multi-chamber bag having a bag body that has a strong seal part that joins two sheet members together to define an interior space of the bag body, and a weak seal part that joints the two sheet members together so as to be able to rupture them apart, thereby partitioning the interior space of the bag body into a medicinal-substance accommodation chamber and a diluting-solution accommodation chamber, a pair of cover sheets are provided to respectively cover the medicinal-substance accommodation chamber.

Abstract: A pharmaceutical container with an improved peelable seal is provided, wherein the container may be made of a flexible polymeric film and comprises at least one peelable seal comprising at least two substantially straight sections which are connected by a rupture zone (5), The rupture zone of the peelable seal may be curved over its whole length between the straight sections. The container may be used for storing pharmaceutical substances, solutions for dialysis, solutions for infusion and/or agents for nutrition.

Abstract: A flexible multi-chamber container for preparation of medical mixed solutions includes at least three chambers separated from each other by leaktight seams. The chambers are designated to be filled with different solutions and are separated from each other by leaktight seams. At least a part of the first leaktight seam is provided with a separation zone to be opened for fluid transfer from the first chamber into the second chamber. At least a part of the second leaktight seam is provided with a separation zone to be opened for fluid transfer from the second chamber into the third chamber. The leaktight seams are arranged and the separation zones are formed such that, in use of the container for preparation of the medical mixed solution, the first separation and second separation zones are opened in a sequential order. The first zone is opened before the second separation zone is opened. Thus, the components are mixed one after another in a predetermined sequential order.

Abstract: In a peritoneal dialysis embodiment of the present invention, spent dialysate from the patient's peritoneal cavity passes, along a patient loop, through a dialyzer having a membrane that separates waste components from the spent dialysate, wherein the patient loop returns fresh dialysate to the patient's peritoneal cavity. The waste components are carried away in a second regeneration loop to a regeneration unit or sorbent cartridge, which absorbs the waste components. The regeneration unit removes undesirable components in the dialysate that were removed from the patient loop by the dialyzer, for example, excess water (ultrafiltrate or UF), toxins and metabolic wastes. Desirable components can be added to the dialysate by the system, such as glucose and electrolytes. The additives assist in maintaining the proper osmotic gradients in the patient to perform dialysis and provide the necessary compounds to the patient.

Abstract: A method and apparatus for separating at least two discrete volumes of a composite liquid into at least a first component and a second component and automatically washing at least one component on a centrifuge rotor. The method comprises transferring a wash solution from a wash solution bag on the rotor into a separation bag; mixing the wash solution and a separated blood component; separating and then transferring the sedimented wash solution into a wash solution discard bag on the rotor. The separated blood component may be washed a plurality of times. A disposable set of tube-connected bags comprises a primary bag, initially containing whole blood, connected to at component bags for receiving plasma or platelets and also connected to a wash solution bag and a wash solution discard bag. The disposable set may further comprise a red blood cell collection bag connected through a filter.

Abstract: An IV infusion bag carrier pack is arranged as a substantially hollow, flexible bag having an interior that is divided into two interior compartments by a flexible, heat permeable divider panel, one interior compartment being arranged to receive and confine an IV fluids bag and the other interior compartment arranged to receive and confine the inflatable pressure cuff member of a blood pressure apparatus, whereby an IV fluids bag contained in the first pocket may be selectively pressurized by inflation of the blood pressure cuff contained in the second pocket whereby selectively controlled infusion delivery of IV fluids contained in the carrier pack apparatus may be continuously maintained irrespective of the relative disposition of the carrier pack apparatus and patient during treatment, extrication and rescue in the field, and transport to a medical facility.

Abstract: The present invention refers to a multicompartment container configured to contain a medical solution. A first compartment is defined by a first peelable seal having a first length extension, L1, and a second peelable seal having a second length extension, L2. A second compartment is defined by the first peelable seal and a third peelable seal having a third length extension, L3. A third compartment is defined by the second and the third peelable seal. The first, second, and third peelable seals are joined and L1>L2+L3. The third compartment comprises a first angle, ?, between an inner side edge of the container and the third peelable seal ranging between 10°<?<80° and the first compartment comprises a second angle, ?, between the first and second peelable seals ranging between 20°<?<130 °.

Abstract: It is an object of the present invention to provide a drug container excellent in unsealability, gas barrier property, contamination resistance, heat resistance, antiblocking property and transparency, and to provide a multilayer film for production of the drug container. To achieve the object, the drug container is formed, for example, of a multilayer film including a first layer (1) composed of a linear ethylene/?-olefin copolymer having a density of 0.930 to 0.950 g/cm3, a second layer (2) and a fourth layer (4) each composed of a mixture containing a linear ethylene/?-olefin copolymer having a density of 0.860 to 0.920 g/cm3 and a linear ethylene/?-olefin copolymer having a density of 0.930 to 0.950 g/cm3 in a weight ratio of 95:5 to 40:60, a third layer (3) composed of a polycycloolefin, and a fifth layer (5) composed of a mixture containing a polyethylene and a polypropylene, the fifth layer 5 serving as an innermost layer.

Abstract: The invention provides container systems, kits and methods for peritoneal dialysis (PD) solutions. Such a system, for example, includes a first compartment that contains a PD osmotic agent and a second compartment that contains a PD buffer agent. The compartments maintain their respective contents separately from one another for purposes of transport, storage and/or sterilization. However, the compartments are fluidly couplable, so that their respective contents can be combined with one another, e.g., following sterilization of the agents and prior to their introduction into the patient's abdomen. The invention provides, in other aspects, such systems, kits and methods that provide protective structure which inhibits breaking of a seal prior between the second compartment and an outlet of the system, prior to breaking of a seal between the first and second compartments.

Abstract: A bicompartment bag adapted to prepare a liquid solution has an assembly of two flexible outer sheets with an access bushing affixed through one of the sheets. The interior of the bag is divided into two chambers by a third flexible sheet having a screen-like stripe with its distal end located at the bottom of the bag. The third sheet has a bore affixed around its edge onto the annular plane of the bushing end projecting into the bag. The first chamber communicates with, through the bushing, a solvent inlet and is partially filled with powdered solute. The inside of the second chamber has a layer separate from the bag. The second chamber layer, constructed of a woven or injected material, extends from a semicircular recess made in correspondence with the bushing to the bottom of the second chamber. The bushing provides the opening for removal of the resulting solution.

Abstract: The disclosure relates to a connector for packaging containing medical fluids, in particular infusion or transfusion bags, including a tubular connection part for receiving a spike for the withdrawal of fluid, and having a lower opening on the packaging side and an upper opening on the connection side. A self-sealing membrane, which is pierced by the spike, is located in the connection part. The membrane has an upper, annular section leading into a lower, plate-shaped section, said annular section of the membrane surrounding the spike in a sealing manner, when the latter pierces the plate-shaped section. The membrane acts as a guide for the spike and also reseals the connector, once the spike has been removed.

Abstract: The present invention relates to a multilayer film for medical solution container and a container comprising the same, more particularly, to the multilayer film for medical solution comprising an outer layer comprising polypropylene, polypropylene copolymer or a mixture thereof; an intermediate layer comprising a mixture of 30˜70% by weight of propylene-based polymer including polypropylene, polypropylene copolymer or a mixture thereof, and 30˜70% by weight of a thermoplastic elastomer; and an inner layer comprising a mixture of 50˜70% by weight of propylene-based polymer including polypropylene, polypropylene copolymer or a mixture thereof, 5˜20% by weight of polyethylene, and 10˜45% by weight of a thermoplastic elastomer.

Abstract: Methods and apparatus for collecting blood samples in vacuum sample tubes are disclosed. The samples, including the initial blood sample, are substantially free of excess air.

Abstract: A novel apparatus and device is described for reconstituting a bone sample with a biological fluid, such as concentrated plasma or saline solutions, for example, prior to surgical implantation into a patient. In particular, the invention comprises, in certain aspects, a container in which a bone sample may be reconstituted with the desired fluid by applying a vacuum within the container, thereby driving the fluid into the bone for complete, or near complete, permeation of the fluid into the interstices of the bone sample prior to surgical implantation.

Abstract: Films having peel seal layers and/or barrier layers are provided. In a general embodiment, the present disclosure provides a film comprising a barrier layer comprising a caprolactam-free nylon compound.

Abstract: An enteral feeding device, includes a system for delivering liquid nutrients to an enteral feeding tube. The device includes: (a) a container, having first, second and third openings; (b) a tip configured to be coupled to the container, the tip having an opening in fluid communication with the first opening of the container, the second opening of the container configured such that nutrient can be delivered to the second opening and the third opening configured to receive nutrient or to allow gas expelled from the patient (e.g., through burping) to flow there through.

Abstract: A blood chamber for an extracorporeal blood circuit comprises a blood inlet port (2), a blood containment chamber (3), a first conduit (8) which connects the blood inlet port (2) with the blood containment chamber (3) and which has an end tract (8a) that terminates in the blood containment chamber (3) with a horizontal inlet component. The first conduit (8) comprises a pre-terminal tract (8b) which precedes the end tract (8a) and which has at least a second horizontal component which is directed in an opposite direction to the horizontal inlet component. The blood chamber is used in an arterial line of a dialysis set for guaranteeing a regular and gentle blood flow.

Abstract: The present invention has an object to provide an infusion container with multiple chambers, where the peel strength of the boundary portion between one and another of multiple medicament chambers is stabilized irrespective of the construction material and structure of the film. The present invention provides an infusion container 10 with multiple chambers, which is formed from a thermoplastic resin film and has a plurality of medicament chambers 11 and 12 for housing medicaments, wherein the medicaments chambers 11 and 12 are liquid-tightly sealed by a peelable weak seal part 15, the weak seal part 15 is formed to have a plurality of melt-bonding parts different in the melt-bonding strength, the strong melt-bonding part having a largest melt-bonding strength among these melt-bonding parts is dispersed and distributed in the weak seal part 15, and the total occupied area of the strong melt-bonding part is less than 25% of the area of the weak seal part 15.

Abstract: The container according to the invention for use in enteral nutrition is characterized in that the container is a multi-chamber bag with at least two chambers separated from one another, wherein at least one chamber contains an enteral nutritive solution with a first energy content and at least one chamber contains a fluid for covering the fluid requirement with an energy content which is less than the energy content of the enteral nutritive solution. Since, with the multi-chamber bag according to the invention, both the enteral nutritive solution and the fluid also required for covering the fluid requirement are made available directly, the application in the case of enteral nutrition is simplified.

Abstract: The present invention relates to a process of fusion-bonding a plastic film (8a, 8b) to an object to be fusion-bonded such as a port member (16) in manufacturing a drug bag, and relates to a drug bag. The present fusion-bonding process comprises steps of disposing a heat generation element generating heat by absorbing infrared laser, on an opposite surface (8c) of the plastic film (8a, 8b) from the port member (16), or between the port member (16) and the plastic film (8a, 8b), pressing a press member (30a, 30b), which allows infrared laser to be transmitted therethrough, from a side of the plastic film (8a, 8b), and irradiating the infrared laser (L) to the heat generation element (24a, 24b) through the press member (30a, 30b).

Abstract: A multi-chamber container having an outlet port, which is usually closed and is opened in cooperation with an expanded deformation of the bag upon the opening of the medical bag and aiming to obtain more reliable opening of the medical bag upon the separation of the partition wall. The outlet port firmly welded to a strong seal 14-1 at an outer periphery has a base portion 12-1, from which a rectangular cross-sectional shaped portion 12-6 integrally extends. The rectangular cross-sectional shaped portion 12-6 has, at its top surface, a U-shaped groove, the bottom surface 30 of which functions as a weak portion 30?. To a portion 33 inward from the U-shaped groove 39 at the top wall of the rectangular cross-sectional shaped portion 12-6, the opposed surface of the medical bag is firmly welded by a point seal 34.

Abstract: A pliable plastic film according to the present invention comprises a heat sealable sealing layer, wherein the sealing layer is made of a mixture of a propylene-?-olefin random copolymer having a crystalline melting point Tm of 135 to 145° C. and a polypropylene (PP) homopolymer having a crystalline melting point Tm of higher than 160° C.

Abstract: Polymer composition comprising a thermoplastic elastomer including styrene and isoprene and/or vinylisoprene units (SI) and a syndiotactic polypropylene (s-PP).

Abstract: A filter for the removal of substances from blood product has a porous element of a polymeric material consisting of a polyether-ester copolymer or of a polymer blend comprising said copolymer.

Abstract: An oxygen-carrying blood substitute preparation stable upon storage is provided. The preparation comprises an oxygen-carrying substance capable of reversibly binding and releasing oxygen in vivo and an amount of a physiologically tolerable reducing agent effective for preventing at least partially irreversible oxidation of said oxygen-carrying substance. Preferably the oxygen-carrying substance is a hemoglobin-based substance in the form of a liposome encapsulating hemoglobin.

Abstract: A medical bag formed of a flexible material includes a front bag part and a rear bag part joined together to form a bag body. A closable liquid inlet port is provided in an upper part of the bag body. The medical bag further includes a deformable elongated member provided in the vicinity of the liquid inlet port on at least one of the front and rear bag parts. The elongated member is deformable so as to retain the liquid inlet port in an open configuration when the elongated member is in a deformed state.