Abstract: In a connection device, when a cannula holding member is in a use state, a position of an end portion of an outer cylindrical portion on a retracted position side does not protrude to the retracted position side, with respect to a position of an end portion of an inner cylindrical portion on the retracted position side. Thereby, a connection device including a structure capable of holding a vial by holding means irrespective of the size of the vial can be provided.

Abstract: A medical device made of an ester resin, such as a hollow-fiber-type blood treatment device, is put into a packaging material made of a gas-impermeable material, and, with at least a reducing gas, such as hydrogen gas, being further enclosed therein, the packaging material is hermetically sealed to provide a medical device package. The medical device package is exposed to radiation to sterilize the inside thereof. In the medical device package, an oxygen scavenger may be further enclosed. The reducing gas may be mixed with an inert gas and enclosed as a mixed gas. As a result, it becomes possible to effectively suppress the generation of by-products, such as acetic acid, from the ester resin.

Abstract: The invention provides a blood purifier which shows a decreased amount of hydrogen peroxide extracted from its selectively permeable separation membranes, and thus is highly reliable in its safety in use for hemecatharysis. The blood purifier comprises selectively permeable separation membranes as a main component and is characterized in that the amount of hydrogen peroxide which is extracted from the selectively permeable separation membrane removed from the blood purifier after 3 months or longer has passed since the sterilization of the blood purifier by exposure to a radioactive ray and/or an electron ray is not larger than 10 ppm.

Abstract: Objects of the invention are to provide a blood purifier package which shows a less increase in the amounts of extracts from the materials of its blood purifier, particularly of its selective permeable separation membranes, attributed to the deterioration of the same materials with time after exposure to a radioactive ray or an electron ray, and which is therefore highly reliable in safety in use for hemocatharsis, and to provide a process for manufacturing the same. The present invention relates to a blood purifier package obtained by packing a blood purifier which comprises selectively permeable separation membranes as a main component, and this blood purifier package is characterized in that the blood purifier is packed and sealed together with an oxygen scavenger in a packaging material capable of shutting out an external air and a water vapor, under a condition of a relative humidity of above 40% RH at 25° C.

Abstract: A foreign matter detecting apparatus includes an oscillating unit, an optical system, a receiving unit, a scanning mechanism, and an operator. The oscillating unit generates a terahertz pulse wave and emits the terahertz pulse wave as irradiation light. The optical system guides the irradiation light to the first part of the container and condenses reflected light from the container. The receiving unit outputs a signal corresponding to the condensed reflected light and also measures an echo. The scanning mechanism scans a position of the irradiation light guided on the first part in a two-dimensional manner. The operator detects foreign matter in powder in a container based on at least one of a time waveform signal, a reflection image, a power spectrum, a tomographic image, and a frequency image. The time waveform signal is output from the receiving unit in chronological order.

Abstract: An indwelling catheter including: a hollow catheter base having a tip and a back end, the back end being able to receive and connect a male connector; a tube provided at the tip of the catheter base; a flexible hemostasis valve installed inside the catheter base; a pusher installed at a back of the hemostasis valve; and a pusher guide installed between the pusher and the catheter base. The pusher has a hollow constitution whose taper reduces in diameter facing its tip. The pusher guide is able to restrict a position of the pusher at a first position where the pusher does not push open the hemostasis valve and a second position where the taper of the pusher is positioned inside the hemostasis valve and pushes open the hemostasis valve.

Abstract: A medical tube clamp wherein first and second plate parts including, on opposing surfaces, compressive protrusions for closing a medical tube are provided with a pair of side walls on both sides projecting from one toward an other of the plate parts, and are also provided with a central guide protrusion projecting from the other toward the one of the plate parts. Both sides of a tip portion of the central guide protrusion make sloping guide surfaces projecting toward a center. When the plate parts are displaced relative to each other so as to become closer, lateral displacement of them is corrected by a slide of the pair of side walls and the sloping guide surfaces, and the central guide protrusion is inserted between the pair of side walls.

Abstract: Objects of the present invention are to provide a blood purifier package which shows a less increase in the amounts of extracts from the materials of its blood purifier, particularly of its selective permeable separation membranes, attributed to the deterioration of the same materials with time after exposure to a radioactive ray or an electron ray, and which is therefore highly reliable in safety in use for hemocatharsis, and to provide a process for manufacturing the same. The present invention relates to a blood purifier package obtained by packing a blood purifier which comprises selectively permeable separation membranes as a main component, and this blood purifier package is characterized in that the blood purifier is packed and sealed together with an oxygen scavenger in a packaging material capable of shutting out an external air and a water vapor, under a condition of a relative humidity of above 40% RH at 25° C.

Abstract: A needle assembly 1 includes a hub 4 retaining a cannula 3, a protective unit 5 advancing and retracting to surround the forward end of the cannula 3, and a cylindrical portion 6 surrounding the outer periphery of the protective unit 5; the protective unit 5 has a construction in which a protective cover 7 protruding from and retracting into the cylindrical portion 6 is formed integrally with a spring portion 8 so as to be in series therewith, with the hub 4 and the cylindrical portion 6 being coupled together to form a hub member.

Abstract: The present invention provides a method for sterilizing a blood purifier, which method is effective to decrease the amounts of extracts from the blood purifier attributed to the deterioration of the selectively permeable separation membranes with time during and after exposure to a radioactive ray or an electron ray, and which method is highly reliable in safety when employed for hemocatharsis therapy. The present invention also provides a blood purifier package. The present invention relates to a method for sterilizing a blood purifier which comprises substantially dried selectively permeable separation membranes as a main component, by way of the exposure of the same blood purifier to a radioactive ray and/or an electron ray, and this method is characterized in that the blood purifier is sealed in a packaging bag, together with an oxygen scavenger and a humectant or together with an oxygen scavenger capable of releasing a moisture, and is then sterilized in such a sealed state by the above exposure.

Abstract: The present invention provides a blood purifier which shows a decreased amount of hydrogen peroxide extracted from its selectively permeable separation membranes, and thus is highly reliable in its safety in use for hemecatharysis. The present invention relates to a blood purifier which comprises selectively permeable separation membranes as a main component and which is characterized in that the amount of hydrogen peroxide which is extracted from the selectively permeable separation membrane removed from the blood purifier after 3 months or longer has passed since the sterilization of the blood purifier by exposure to a radioactive ray and/or an electron ray is not larger than 10 ppm.

Abstract: Provided is a platelet-rich plasma separator which can carry out the separation of a platelet-rich plasma with a small number of gamma radiation sterilized instruments and a platelet-rich plasma separation method. The platelet-rich plasma separator comprises a first syringe and a second syringe. The first syringe comprises a first syringe cylinder provided with a first port on which a blood collection needle can be mounted, a first cap detachable from the first port, a first gasket for sealing the first syringe cylinder fluid-tightly, which first gasket is reciprocated within the first syringe cylinder, and a first plunger provided detachably on the first gasket.

Abstract: A medical connector capable of allowing, in which a stepped portion is not formed between upper surfaces of a valve and a housing, includes a disc shaped valve member which has a slit formed at a center portion thereof; a housing with a substantially cylindrical shape which sandwiches a circumferential edge portion of the valve member; and an annular ring member which is disposed on an upper circumferential edge of the valve member other than the center portion thereof, wherein the housing has a pedestal which is formed on an inner circumferential surface thereof so as to protrude inward, the valve member being placed on the pedestal, and wherein the valve member is fixed to the inside of the housing by allowing the ring member and the housing to be joined to each other by a swaging process after the valve member is placed on the pedestal in the housing.

Abstract: An infusion pump includes a pump body for holding a roller clamp 7, and a roller movement mechanism 3 for moving a roller 72 of the roller clamp 7 and operating in coordination with manipulation of a door lock mechanism. When the door lock mechanism is in an unlocked state, an infusion tube T is blocked by the roller clamp 72. This configuration reliably prevents free flow even if a door is not closed completely or if the door is accidentally left unlocked. After the finish of infusion treatment, the infusion tube T is blocked by the roller clamp 7 at the moment when the door lock mechanism is unlocked before the opening of the door. This configuration avoids a trouble of removing the infusion tube T from the infusion pump while a user forgets to block the infusion tube by the roller clamp 7.

Abstract: The present invention relates to glucose dehydrogenase [NAD(P)+GDH] using nicotinamide adenine dinucleotide or nicotinamide adenine dinucleotide phosphate as a coenzyme, in which the thermal stability and/or the resistance to an organic solvent in the absence of sodium chloride are improved.

Abstract: It is intended to provide a thrombus-aspiration catheter capable of exerting flexibility and aspiration force even in the case where the tube in the front end side is a triple lumen tube or a contrast marker is provided at the front end. A thrombus-aspiration catheter (1) comprising a basal end side tube (2) of the double lumen type which has an aspiration lumen (11) and a core wire lumen (12), and a front end side tube (3) of the triple lumen type which has a guide wire lumen (13) in addition to the aspiration lumen (11) and the core wire lumen (12), wherein the front end of the above-described front end side tube is obliquely cut and a terminal aspiration tube (4) of a flexible double lumen, which has a front end opening (41) inclined in almost the same direction as the cut face (31), is connected to the cut face.

Abstract: A medical hollow needle structured in accordance with the present invention, wherein the puncture resistance of a blade surface over the entire length in the puncture direction can be made substantially equal, and the patient's pain during needle puncture can be relieved due to a reduction in the peak level of puncture pain with the duration of sensory awareness of the puncture pain shortened by the use of the blade surface in a novel shape employing, in combination with each other, first to fourth inclined surfaces having specific inclination directions. Accordingly, the present invention provides a medical hollow needle with a blade surface in a novel shape whereby the puncture pain can be further reduced compared to needles with a conventional structure, and to provide a preferred method of producing such a medical hollow needle.

Abstract: An electrode pad for use on a living organism can measure an electrocardiographic signal without being hindered by body-motion noise. The electrode pad is attached to the skin of the living organism, detects an electrical signal, and supplies the electrical signal to an electrocardiograph. The electrode pad for use on a living organism is characterized by the provision of a mesh-like electrode that extends along the skin, a conductive gel sheet that is layered on top of the electrode and extends along the surface of the skin, and a soft protective sheet that covers the layered electrode and conductive gel sheet.

Abstract: A method for producing a vial with low alkali elution by removing a deteriorated region caused by processing on an internal surface of a vial is disclosed. The method is for forming vials from borosilicate glass tubes with a bottom wherein an internal surface of the tube is fire-blasted with a flame.

Abstract: An indwelling needle assembly and protector. The indwelling needle assembly has an inner needle, an inner needle hub, an outer needle, an outer needle hub, and a protector for protecting the needle point of the inner needle arranged on the outer periphery of the inner needle so as to be slidable in the axial direction. The protector includes a protecting member in which the needle point of the inner needle is stored and a closing member arranged on the outer periphery of the protecting member so as to be capable of sliding, a displaceable side wall which is capable of being displaced inward so as to close a distal opening of the protecting member, the displaceable side wall being displaced inwardly by the closing member arranged on the outer periphery of the distal end portion of the protecting member.