WO2013125443A1 - 医療用具梱包体 - Google Patents
医療用具梱包体 Download PDFInfo
- Publication number
- WO2013125443A1 WO2013125443A1 PCT/JP2013/053539 JP2013053539W WO2013125443A1 WO 2013125443 A1 WO2013125443 A1 WO 2013125443A1 JP 2013053539 W JP2013053539 W JP 2013053539W WO 2013125443 A1 WO2013125443 A1 WO 2013125443A1
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- WO
- WIPO (PCT)
- Prior art keywords
- medical device
- syringe
- sealing member
- adhesive
- container body
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/002—Packages specially adapted therefor, e.g. for syringes or needles, kits for diabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/001—Apparatus specially adapted for cleaning or sterilising syringes or needles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
- A61M5/3202—Devices for protection of the needle before use, e.g. caps
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B55/00—Preserving, protecting or purifying packages or package contents in association with packaging
- B65B55/02—Sterilising, e.g. of complete packages
- B65B55/04—Sterilising wrappers or receptacles prior to, or during, packaging
- B65B55/10—Sterilising wrappers or receptacles prior to, or during, packaging by liquids or gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B55/00—Preserving, protecting or purifying packages or package contents in association with packaging
- B65B55/02—Sterilising, e.g. of complete packages
- B65B55/12—Sterilising contents prior to, or during, packaging
- B65B55/18—Sterilising contents prior to, or during, packaging by liquids or gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B7/00—Closing containers or receptacles after filling
- B65B7/16—Closing semi-rigid or rigid containers or receptacles not deformed by, or not taking-up shape of, contents, e.g. boxes or cartons
- B65B7/28—Closing semi-rigid or rigid containers or receptacles not deformed by, or not taking-up shape of, contents, e.g. boxes or cartons by applying separate preformed closures, e.g. lids, covers
- B65B7/2842—Securing closures on containers
- B65B7/2878—Securing closures on containers by heat-sealing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D1/00—Containers having bodies formed in one piece, e.g. by casting metallic material, by moulding plastics, by blowing vitreous material, by throwing ceramic material, by moulding pulped fibrous material, by deep-drawing operations performed on sheet material
- B65D1/22—Boxes or like containers with side walls of substantial depth for enclosing contents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
- B65D25/02—Internal fittings
- B65D25/10—Devices to locate articles in containers
- B65D25/108—Devices, e.g. plates, presenting apertures through which the articles project
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D43/00—Lids or covers for rigid or semi-rigid containers
- B65D43/02—Removable lids or covers
- B65D43/0202—Removable lids or covers without integral tamper element
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D77/00—Packages formed by enclosing articles or materials in preformed containers, e.g. boxes, cartons, sacks or bags
- B65D77/10—Container closures formed after filling
- B65D77/20—Container closures formed after filling by applying separate lids or covers, i.e. flexible membrane or foil-like covers
- B65D77/2024—Container closures formed after filling by applying separate lids or covers, i.e. flexible membrane or foil-like covers the cover being welded or adhered to the container
Definitions
- the present invention relates to a medical device package that stores medical devices such as a syringe and a connector.
- a syringe storage container that can hold and store a plurality of syringes in an upright state is widely used for transporting or storing a syringe before being filled with a chemical solution or the like.
- a syringe storage container includes a box-shaped container body whose upper surface is opened, a holder that holds a plurality of syringes in an upright state, and a sealing member that seals the opening of the container body. .
- a shelf-like part that supports the holder is provided inside the container body.
- the holder is formed in a plate shape having a plurality of through holes, and the syringe is inserted by inserting the syringe into the through hole of the holder and hooking the flange portion provided at the syringe end to the peripheral edge of the through hole. It is held by the holder.
- a syringe storage container it is possible to hold a plurality of syringes upright and in a state where the filling port for the chemical solution is directed upward.
- the syringe is manufactured at a place different from the place where the chemical solution is filled.
- the manufactured syringe is housed in a syringe housing container, and the opening of the syringe housing container is sealed with a sealing member to assemble the medical device package. Thereafter, high-temperature steam sterilization (autoclave), EOG (ethylene oxide gas) sterilization, or the like is allowed to pass through the sealing member to sterilize the syringe container.
- autoclave autoclave
- EOG ethylene oxide gas
- the syringe storage container that has been sterilized is transported to a place where the chemical solution is filled.
- the sealing of the syringe storage container by the sealing member is opened, the holder holding the plurality of syringes is taken out from the container body, and set in the chemical solution filling device. Thereafter, the syringe is filled with the chemical solution.
- the medical container described in Patent Document 1 includes a tray that supports the syringe chest, a tank in which the tray is fitted, a protective sheet that covers the tray and the syringe barrel, and a cover sheet that seals the tank.
- the cover sheet is a gas permeable material such as a non-woven polyolefin and is releasably bonded to the tank flange.
- the adhesive applied to the cover sheet is applied to one surface facing the flange of the tank.
- the protective sheet is disposed in the tank so that bacteria, dust, and the like do not enter the syringe after the cover sheet is peeled from the tank.
- the protective sheet is adhered to the cover sheet, the protective sheet is removed together with the cover sheet when the cover sheet is peeled off from the tank. Therefore, when the cover sheet is peeled from the tank, the syringe is exposed, and there is a possibility that bacteria, dust, and the like enter the syringe.
- the protective sheet when removing the cover sheet from the tank in an environment free from bacteria and dust, the protective sheet may not be used.
- the sterilization process is performed in the tank using high-temperature steam or gas
- the surface of the cover sheet to which the adhesive is applied comes into contact with the syringe.
- the syringe is adhered to the cover sheet, or the adhesive is transferred to the syringe and adhered as a foreign substance, which is not preferable.
- the present invention has been made in view of the above points, and even if a sterilization process in a tank (container body) is performed using steam or gas, a cover sheet (sealing) is applied to the protective sheet or medical device in the tank. It is an object of the present invention to provide a medical device package to which the adhesive of (member) does not adhere.
- the medical device package of the present invention comprises a medical device having one end surface and the other end surface, and a medical device storage container for storing the medical device.
- the tool storage container includes a container body and a sheet-like sealing member.
- the container body includes a peripheral wall portion having an upper end portion and a lower end portion, a bottom portion continuous with the lower end portion, surrounded by the lower end portion, an opening portion surrounded by the upper end portion, a peripheral wall portion, a bottom portion, and an opening portion.
- the sealing member is bonded to the container body and seals the opening of the container body.
- the surface of the sealing member that faces the container body has an adhesive application area where an adhesive is applied and an adhesive non-application area where no adhesive is applied.
- region is an area
- the adhesive non-application region of the sealing member is set to a region facing at least one end surface of the medical device held by the holding unit. Therefore, when the sealing member is pressed by steam or gas during sterilization and deformed to be recessed inside the container body, even if the sealing member comes into contact with one end surface of the medical device held by the holding part, Adhesive does not adhere to medical devices. As a result, the medical device is not bonded to the sealing member, and the medical device can be kept in a good state. In addition, when an inner sheet (protective sheet) is disposed between the medical device and the sealing member, the adhesive does not adhere to the inner sheet even if the sealing member contacts the inner sheet.
- a medical device package comprising a medical device having one end surface and the other end surface, and a medical device storage container for storing the medical device
- the medical device storage container is: A peripheral wall portion having an upper end portion and a lower end portion; a bottom portion continuous to the lower end portion and surrounded by the lower end portion; an opening portion surrounded by the upper end portion; the peripheral wall portion, the bottom portion and the opening portion
- a container body having a holding portion for holding the medical device provided in the storage space and holding the medical device so that the one end surface faces the upper end;
- a sheet-like sealing member that is bonded to the container body and seals the opening of the container body,
- the surface of the sealing member that faces the container body has an adhesive application region to which an adhesive is applied, and an adhesive non-application region to which no adhesive is applied, and the adhesive non-application region is A medical device package that is a region facing at least one end surface of the medical device held by the holding unit.
- the medical device is a syringe having one end face and the other end face, and provided with a filling port for filling the one end face with a chemical solution
- the holding portion includes a syringe holding member that engages with an inner surface of the peripheral wall portion and faces the bottom portion, and holds the syringe so that the one end surface of the syringe faces an upper end. Medical device packaging.
- region is a medical device package as described in (3) which is an area
- the container body has a flange portion that is continuous with the upper end portion and surrounds the upper end portion,
- the medical device package of the present invention it is possible to prevent the adhesive from adhering to the medical device in the container body even when the container body is sterilized using steam or gas.
- FIG. 1 is a perspective view of a medical device package according to a first embodiment of the present invention. It is a disassembled perspective view of the medical device package which concerns on the 1st Embodiment of this invention. It is a perspective view of the container main body in the medical device package which concerns on the 1st Embodiment of this invention. It is a perspective view of the sealing member in the medical device package which concerns on the 1st Embodiment of this invention. It is a fragmentary longitudinal cross-sectional view of the medical device package which concerns on the 1st Embodiment of this invention. It is a perspective view of the sealing member in the medical device package which concerns on the 2nd Embodiment of this invention.
- FIG. 1 is a perspective view of the medical device package according to the first embodiment.
- FIG. 2 is an exploded perspective view of the medical device package according to the first embodiment.
- the syringe package 80 which shows the medical device package which concerns on 1st Embodiment is the syringe storage container 1 which shows a specific example of a medical device storage container, and the syringe storage container 1. It is comprised from the syringe 10 (refer FIG. 2) which shows one specific example of the medical device accommodated in.
- the syringe storage container 1 is used when simultaneously transporting and storing a plurality of syringes 10.
- the syringe storage container 1 includes a syringe holding member 30 that holds a plurality of syringes 10, a container body 40 that stores a syringe holding member 30 that holds a plurality of syringes 10, a sealing member 50, and an inner sheet 60. ing.
- the syringe holding member 30 shows a specific example of the holding unit according to the present invention, and holds the syringe 10 in a state where a filling port 15 described later is directed upward.
- the syringe holding member 30 is placed on a mounting shelf 44 (see FIG. 3), which will be described later, of the container body 40, and is opposed to a bottom 41, which will be described later, of the container body 40.
- the syringe holding member 30 has a rectangular and flat base plate 31 and a cylindrical portion 32 protruding from one surface of the base plate 31.
- the base plate 31 is provided with a plurality of through holes 31a (see FIG. 5) for inserting the syringe 10.
- the through-hole 31a is formed in a circular shape, and its diameter is larger than the outer diameter of a syringe body 11 described later in the syringe 10.
- the plurality of through holes 31 a are arranged on the base plate 31 in a staggered manner. Thereby, since the distance between the adjacent through-holes 31a becomes equal, it can suppress that the adjacent syringe 10 contacts during conveyance of the syringe storage container 1.
- notches 31b are formed on the two opposing sides of the base plate 31, respectively. The user can easily remove the syringe holding member 30 locked to the container body 40 by inserting a finger into the notch 31b.
- the cylinder part 32 is formed so as to cover the through hole 31a of the base plate 31, and has a cylinder hole 32a (see FIG. 5) for inserting the syringe 10.
- the cylindrical hole 32a communicates with the through hole 31a.
- the diameter of the cylindrical hole 32a is substantially equal to the diameter of the through hole 31a.
- a flange portion 16 described later of the syringe 10 is engaged with the cylindrical portion 32.
- the inner sheet 60 is formed in a rectangular sheet shape.
- the area of the inner sheet 60 is set to a size that covers a later-described filling port 15 side of the syringe 10 held by the syringe holding member 30.
- the inner sheet 60 is placed on a flange portion 16 described later of the syringe 10 held by the syringe holding member 30.
- the inner sheet 60 is preferably permeable to gas for sterilization and impermeable to fine particles such as bacteria and viruses.
- Examples of the material for the inner sheet 60 include Tyvek (registered trademark), which is a high-density polyethylene nonwoven fabric manufactured by DuPont.
- Tyvek registered trademark
- the sealing member 50 formed with the high density polyethylene nonwoven fabric becomes opaque.
- FIG. 3 is a perspective view of the container body 40.
- the container body 40 includes a peripheral wall portion 42 having an upper end portion and a lower end portion, a bottom portion 41 continuous with the lower end portion of the peripheral wall portion 42 and surrounded by the lower end portion, and an upper end of the peripheral wall portion 42.
- the internal space of the container body 40 surrounded by the peripheral wall portion 42, the bottom portion 41, and the opening 40a serves as a storage space for storing the syringe holding member 30 and the syringe 10.
- the bottom 41 is formed in a substantially rectangular plate shape and constitutes the lower end of the container body 40.
- the size of the inner surface 41 a in the bottom 41 is smaller than the base plate 31 in the syringe holding member 30.
- the flange 43 is substantially orthogonal to the upper end of the peripheral wall portion 42 and is formed in a rectangular frame shape.
- the flange 43 has an upper surface 43a facing the upper end and a lower surface 43b facing the lower end.
- the upper surface 43a and the lower surface 43b are formed in a plane.
- a protrusion 45 is formed on the upper surface 43 a of the flange 43.
- the protrusion 45 is provided so as to surround the opening 40 a and is formed endlessly along the flange 43. That is, the protrusion 45 is formed over the entire circumference of the flange 43.
- a sealing member 50 (see FIG. 2) is fused (adhered) to the protruding portion 45.
- the width of the protrusion 45 is set to be smaller than the width of the flange 43.
- the width of the protrusion 45 is preferably 2 to 10 mm in consideration of sealing the inside of the syringe container by securely fusing the sealing member 50.
- the height of the protrusion 45 is preferably 0.2 to 0.5 mm or more.
- the outer contour of the ridge 45 is smaller than the outer contour of the flange 43. For this reason, when the sealing member 50 is placed on the ridge 45, the sealing member 50 is less likely to bend toward the opening 40 a of the container body 40, and the sealing member 50 is reliably placed on the ridge 45. . Therefore, the sealing member 50 can be reliably fused to the protrusion 45. Further, when the sealing member 50 is peeled off, the upper surface of the flange 43 that is outside of the protruding portion 45 can be pressed, so that the sealing member 50 is easily peeled off.
- the contour of the inner periphery of the ridge 45 is larger than the contour of the outer periphery at the upper end of the peripheral wall portion 42. For this reason, when the sealing member 50 is heat-sealed, the sealing member 50 can be reliably fused to the ridge portion 45 because it can be received directly under the ridge portion 45 and supported by a jig (not shown). .
- the protrusion 45 has a square shape 45a.
- the square shapes 45a are arranged at the four corners of the flange 43, and are formed at right angles.
- stress is concentrated on the square shape 45a.
- the sealing member 50 is easily peeled off from the square shape 45a.
- the square shape 45a exists in the four corners of the flange 43, when peeling off the sealing member 50, it can always peel off from the fixed place. The sealing member 50 is not unintentionally peeled from other than the four corners of the flange 43.
- the container body 40 and the syringe holding member 30 are preferably not denatured by sterilization using high-temperature steam or gas such as high-pressure steam sterilization (autoclave) or EOG (ethylene oxide gas) sterilization.
- high-temperature steam or gas such as high-pressure steam sterilization (autoclave) or EOG (ethylene oxide gas) sterilization.
- materials for the container body 40 and the syringe holding member 30 include resins having excellent durability such as polypropylene, polystyrene, polyethylene, polycarbonate, ABS resin, and PET.
- the container main body 40 and the syringe holding member 30 are preferably substantially transparent or translucent in order to ensure the visibility inside the container main body 40. Among these, polycarbonate, polystyrene, and PET are listed.
- FIG. 4 is a perspective view of a state in which the surface of the sealing member 50 facing the container body 40 is directed upward.
- the sealing member 50 is formed in a rectangular sheet shape that is substantially equal to the contour of the outer periphery of the flange 43 (see FIG. 3) in the container body 40. That is, the contour of the outer periphery of the protrusion 45 provided on the flange 43 is formed smaller than the contour of the outer periphery of the sealing member 50.
- the sealing member 50 is heat-sealed to the flange 43 of the container body 40 using an adhesive. Specifically, it is heat-sealed to the protrusion 45 of the flange 43.
- the sealing member 50 is preferably permeable to gas for sterilization and not permeable to fine particles such as bacteria and viruses.
- Examples of the material of the sealing member 50 include Tyvek (registered trademark), which is a high-density polyethylene nonwoven fabric manufactured by DuPont.
- Tyvek registered trademark
- the sealing member 50 formed with the high density polyethylene nonwoven fabric becomes opaque.
- An adhesive application region 50a and an adhesive non-application region 50b are formed on the surface of the sealing member 50 facing the container body 40.
- a thermoplastic adhesive hot melt
- the adhesive application region 50 a comes into contact with a protrusion 45 provided on the flange 43 of the container body 40. Thereafter, the contact portion between the sealing member 50 and the protruding portion 45 is heated by the mold, whereby the adhesive is dissolved and the sealing member 50 and the protruding portion 45 are thermally fused (adhered).
- region 50b is set to the area
- FIG. 5 is a partial longitudinal sectional view of the syringe package 80.
- the syringe 10 includes a syringe body 11 formed of a hollow cylindrical body, a discharge portion 12 formed on the distal end side of the syringe body 11, and a needle tube 13 fixed to the discharge portion 12. is doing. That is, the syringe storage container 1 of the present embodiment stores the syringe 10 with a needle.
- the outer diameter of the syringe body is smaller than the through hole 31a and the cylindrical hole 32a of the syringe holding member 30.
- a liquid chamber for storing the filled chemical liquid is formed inside the syringe body 11.
- a filling port 15 for filling the liquid chamber of the syringe body 11 with a chemical solution is formed on the base end side opposite to the discharge portion 12 of the syringe body 11. In this Embodiment, let the end surface by the side of the filling port 15 of the syringe main body 11 be an end surface, and let the end surface of the discharge part 12 be an other end surface.
- a flange portion 16 having an outer contour formed in an elliptical shape is provided around the filling port 15 of the syringe body 11.
- the flange portion 16 is formed such that at least a part (for example, a long diameter) of the outer diameter is larger than the diameter of the cylindrical hole 32 a in the syringe holding member 30. Therefore, the flange portion 16 of the syringe 10 inserted into the cylindrical hole 32 a and the through hole 31 a is placed on the upper end portion of the cylindrical portion 32.
- the shape of the flange part 16 is not restricted to the elliptical shape of this embodiment, For example, an annular shape may be sufficient.
- a cap member 20 is attached to the discharge portion 12.
- the cap member 20 is formed in a substantially cylindrical shape, and one end in the axial direction is open and the other end in the axial direction is closed.
- the cap member 20 covers the discharge portion 12 and the needle tube 13 protruding from the discharge portion 12.
- Examples of the material of the cap member 20 include elastic members such as rubber and elastomer.
- the syringe 10 is inserted into the through-hole 31 a provided in the syringe holding member 30 with the cap member 20 attached to the discharge unit 12, and is held by the syringe holding member 30.
- the syringe holding member 30 and the container main body 40 are prepared. Then, the base plate 31 of the syringe holding member 30 is placed on the placement shelf 44 of the container body 40. Thereby, the syringe holding member 30 is engaged with the container main body 40.
- the syringe 10 is inserted into the cylindrical hole 32a and the through hole 31a of the syringe holding member 30.
- a cap member 20 is attached to the discharge part 12 of the syringe 10 in advance.
- the syringe 10 to which the cap member 20 is attached is held by the syringe holding member 30 and stored in the container main body 40 (state shown in FIG. 3).
- the inner sheet 60 is placed on the flange portions 16 of the plurality of syringes 10 held by the syringe holding member 30. Thereby, the filling port 15 (flange part 16) side of the plurality of syringes 10 held by the syringe holding member 30 is covered with the inner sheet 60.
- the sealing member 50 is placed on the protrusion 45 provided on the flange 43 of the container body 40. Then, a receiving jig (not shown) is brought into contact with the lower surface 43b of the flange 43, and the sealing member 50 is pressed by a heated mold (not shown). As a result, the adhesive applied to the sealing member 50 is dissolved, the sealing member 50 and the protrusion 45 are thermally fused (adhered), and the syringe package 80 is assembled.
- the thickness of the flange 43 at the portion where the protrusion 45 is provided is ensured.
- the protrusion 45 is not deformed by the applied heat, and the sealing member 50 and the protrusion 45 are reliably heated. It can be fused.
- the mold (not shown) is formed in a rectangular flat plate shape, for example, and presses the entire surface of the sealing member 50. At this time, since only the protrusion 45 contacts the sealing member 50, the sealing member 50 is not thermally fused (adhered) to the region other than the protrusion 45 of the flange 43. That is, the sealing member 50 can always be heat-sealed to the protrusion 45.
- the adhesive application region 50 a (see FIG. 4) formed on the sealing member 50 has a larger area than the flange 43 of the container body 40. Therefore, even if the sealing member 50 is displaced to some extent with respect to the container body 40, the adhesive application region 50 a of the sealing member 50 can be brought into contact with the protrusion 45 on the flange 43 of the container body 40. As a result, even if the sealing member 50 is displaced to some extent with respect to the container body 40, both can be bonded.
- the contour of the outer periphery of the protrusion 45 provided on the flange 43 of the container body 40 is smaller than the contour of the outer periphery of the flange 43 and the sealing member 50, the outer edge portion of the flange 43 and the sealing member 50 is heated. Not fused (sealed). Thereby, when peeling the sealing member 50 from the container main body 40, it becomes easy to hold
- the syringe package 80 After assembling the syringe package 80, the syringe package 80 is packaged with a sterilization packaging bag having an opening, and the opening of the packaging bag is sealed. Subsequently, the syringe package 80 in the syringe package is sterilized using high-temperature steam or gas such as high-pressure steam sterilization (autoclave) or EOG (ethylene oxide gas) sterilization.
- high-temperature steam or gas such as high-pressure steam sterilization (autoclave) or EOG (ethylene oxide gas) sterilization.
- a part of the sterilization packaging bag like the sealing member 50, is made of a material that allows gas for sterilization to pass therethrough and does not allow microparticles such as bacteria and viruses to pass through. For this reason, high-temperature vapor
- sterilization can be performed on the outer surface of the syringe package 80, the syringe holding member 30 inside the syringe package 80, and the syringe 10 held on the syringe holding member 30.
- the sealing member 50 When the sterilization process is performed on the syringe package 80, the sealing member 50 is pressed by high-temperature steam or gas and deformed so as to be recessed inside the container body 40. Thereby, the surface facing the container main body 40 of the sealing member 50 contacts the filling port 15 side of the plurality of syringes 10 held by the syringe holding member 30 with the inner sheet 60 interposed therebetween (see FIG. 5).
- the region facing the filling port 15 side of the plurality of syringes 10 on the surface facing the container body 40 of the sealing member 50 is the adhesive non-application region 50b where no adhesive is applied. That is, the adhesive non-application area 50 b of the sealing member 50 is deformed toward the filling port 15 side of the syringe and contacts the filling port 15 via the inner sheet 60 when sterilized by high-pressure steam. Therefore, the adhesive does not adhere to the inner sheet 60 because the adhesive is not applied to the region of the sealing member 50 that contacts the inner sheet 60. As a result, when the syringe package 80 is opened, the inner sheet 60 is not removed together with the sealing member 50, and the inner sheet 60 can keep the state where the filling ports 15 of the plurality of syringes 10 are covered. .
- region 50a) of the part facing the filling port 15 of the several syringe 10 in the surface facing the container main body 40 of the sealing member 50 is a container main body. 40 is close to the ridge 45 which is a bonding portion with 40. Therefore, it is difficult for the sealing member 50 to be deformed in the direction approaching the filling port 15 of the syringe 10 in the vicinity of the protrusion 45 (adhesion). Thereby, the adhesive application region 50 a of the sealing member 50 is unlikely to contact the inner sheet 60.
- the syringe 10 is not present under the sealing member 50 in the vicinity of the protrusion 45 (adhesion). For this reason, even if the sealing member 50 near the protrusion 45 (adhesive portion) is deformed and comes into contact with the inner sheet 60, the inner sheet 60 is deformed following the sealing member 50, and the sealing member 50 Adhesive does not adhere to the extent that it adheres.
- FIG. 6 is a perspective view of a sealing member in the medical device package according to the second embodiment.
- the medical device package according to the second embodiment has the same configuration as the syringe package 80 (see FIG. 2) of the first embodiment.
- the syringe package of the second embodiment is different from the syringe package 80 only in the sealing member. Therefore, here, the sealing member 51 in the medical device package according to the second embodiment will be described.
- the sealing member 51 shown in FIG. 6 is formed in a rectangular sheet shape that is substantially equal to the contour of the outer periphery of the flange 43 (see FIG. 2) in the container body 40.
- the sealing member 51 is heat-sealed to the flange 43 of the container body 40 using an adhesive. Specifically, it is heat-sealed to the protrusion 45 of the flange 43.
- the sealing member 51 is different from the sealing member 50 according to the first embodiment (see FIG. 4) in an adhesive application region 51a and an adhesive non-application region 51b.
- thermoplastic adhesive hot melt
- the adhesive application area 51a has a smaller area than the adhesive application area 50a (see FIG. 4) of the sealing member 50 according to the first embodiment, but is smaller than the flange 43 (see FIG. 2) of the container body 40. Is also large.
- the adhesive application area 51 a comes into contact with the protrusion 45 provided on the flange 43 of the container body 40. Thereafter, the contact portion between the sealing member 51 and the protrusion 45 is warmed by the mold, so that the adhesive is dissolved and the sealing member 51 and the protrusion 45 are thermally fused (adhered).
- This adhesive non-application area 51b is set in an area facing the inner sheet 60 (see FIG. 2).
- the same effect as the syringe package (medical device package) 80 of the first embodiment can be obtained also in the medical device package of the second embodiment having such a configuration.
- the adhesive application region 51 a formed on the sealing member 51 has a larger area than the flange 43 of the container body 40. Therefore, even if the sealing member 51 is displaced to some extent with respect to the container main body 40, the adhesive application region 51a of the sealing member 51 is brought into contact with the protrusion 45 on the flange 43 of the container main body 40 to bond them together. can do.
- FIG. 7 is a perspective view of a sealing member in the medical device package according to the third embodiment.
- the medical device package according to the third embodiment has the same configuration as the syringe package 80 (see FIG. 2) of the first embodiment.
- the medical device package of the third embodiment is different from the syringe package 80 only in the sealing member. Therefore, here, the sealing member 52 in the medical device package according to the third embodiment will be described.
- the sealing member 52 shown in FIG. 7 is formed in a rectangular sheet shape that is substantially equal to the contour of the outer periphery of the flange 43 (see FIG. 2) in the container body 40.
- the sealing member 52 is heat-sealed to the flange 43 of the container body 40 using an adhesive. Specifically, it is heat-sealed to the protrusion 45 of the flange 43.
- the sealing member 52 is different from the sealing member 50 according to the first embodiment (see FIG. 4) in an adhesive application region 52a and an adhesive non-application region 52b.
- thermoplastic adhesive hot melt
- the adhesive application region 52a has a smaller area than the adhesive application region 50a (see FIG. 4) of the sealing member 50 according to the first embodiment, and is substantially the same as the flange 43 (see FIG. 2) of the container body 40. It is set to an equal area.
- the adhesive application region 52 a comes into contact with the protrusion 45 provided on the flange 43 of the container body 40. Thereafter, the contact portion between the sealing member 52 and the protruding portion 45 is heated by the mold, whereby the adhesive is dissolved and the sealing member 52 and the protruding portion 45 are thermally fused (adhered).
- region 51b is set to the area
- the same effect as the syringe package 80 (medical device package) of the first embodiment can be obtained also in the medical device package of the third embodiment having such a configuration.
- the adhesive application region 51 a formed in the sealing member 52 is set to an area substantially equal to the flange 43 of the container body 40. Therefore, even if the sealing member 52 is displaced to some extent with respect to the container main body 40, the adhesive application region 51 a of the sealing member 51 is brought into contact with the protrusion 45 on the flange 43 of the container main body 40 to bond them together. can do.
- an inner sheet No adhesive adheres to 60.
- the inner sheet 60 is not removed together with the sealing member 52 at the time of opening the second embodiment of the syringe package, and the filling ports 15 side of the plurality of syringes 10 are covered by the inner sheet 60. Can keep the state.
- FIG. 8 is a longitudinal sectional view of a medical device package according to the fourth embodiment.
- FIG. 9 is an exploded view of the medical device package according to the fourth embodiment.
- a needle member package 180 showing a medical device package according to the fourth embodiment includes a needle member storage container 100 showing another specific example of the medical device storage container, and a needle.
- the needle member 110 is shown as another specific example of the medical instrument stored in the member storage container 100.
- the needle member storage container 100 is used when the needle member 110 is transported and stored.
- the needle member storage container 100 includes a container main body 140 that holds and stores the needle member 110 and a sealing member 150.
- the container body 140 includes a peripheral wall portion 142 having an upper end portion and a lower end portion, a bottom portion 141 continuous with the lower end portion of the peripheral wall portion 142 and surrounded by the lower end portion, and an upper end of the peripheral wall portion 142.
- An internal space of the container body 140 surrounded by the peripheral wall 142, the bottom 141, and the opening 140a is a storage space for storing the needle member 110.
- the bottom 141 is formed in a substantially circular plate shape, and constitutes the lower end of the container body 140.
- the peripheral wall 142 is formed in a substantially cylindrical shape, and includes a lower cylinder 145 that is continuous with the bottom 141, a tapered cylinder 146 that is continuous with the lower cylinder 147, and an upper cylinder 147 that is continuous with the tapered cylinder 146. Yes.
- the diameter of the lower cylinder 145 is set smaller than that of the upper cylinder.
- the diameter of the tapered cylinder 146 increases continuously toward the upper cylinder 147 side.
- the inner surface of the tapered cylinder 146 engages with a cap member 120 (described later) attached to the needle member 110.
- a step portion 146 a is formed on the inner surface of the tapered tube 146 on the upper tube 147 side.
- the needle member 110 is held in the container main body 140 by the contact portion 113 of the needle member 110 described later coming into contact with the stepped portion 146a. That is, the step portion 146a shows another specific example of the holding portion according to the present invention.
- the stepped portion 146a may be omitted.
- the cap member 120 described later is engaged with the inner surface of the tapered cylinder 146, whereby the needle member 110 is held in the container main body 140. That is, the inner surface of the tapered cylinder 146 shows another specific example of the holding portion according to the present invention.
- the flange 143 is substantially orthogonal to the upper end of the peripheral wall 142 and is formed in a ring-shaped frame shape.
- the flange 143 has an upper surface 143a facing the upper end and a lower surface 143b facing the lower end.
- the upper surface 143a and the lower surface 143b are formed in a plane.
- the container body 140 is preferably not denatured by sterilization using high-temperature steam or gas such as high-pressure steam sterilization (autoclave) or EOG (ethylene oxide gas) sterilization.
- high-temperature steam or gas such as high-pressure steam sterilization (autoclave) or EOG (ethylene oxide gas) sterilization.
- EOG ethylene oxide gas
- Examples of the material of the container body 140 include resins having excellent durability such as polypropylene, polystyrene, polyethylene, polycarbonate, ABS resin, and PET.
- the sealing member 150 is formed in a sheet shape, and includes a circular portion 150 a and a gripping portion 150 b that is continuous with a part of the circular portion 150.
- the outer diameter of the circular portion 150 a is set to be slightly larger than the outer peripheral contour of the flange 143 in the container main body 140.
- the circular portion 150a of the sealing member 150 is heat-sealed to the flange 143 of the container body 140 using an adhesive.
- the gripping part 150b is formed in a substantially triangular shape with one side continuing to the circular part 150b. The grip 150b is not bonded to the container body 140.
- the sealing member 150 is preferably permeable to gas for sterilization and not permeable to microparticles such as bacteria and viruses.
- Examples of the material of the sealing member 150 include Tyvek (registered trademark), which is a high-density polyethylene nonwoven fabric manufactured by DuPont.
- Tyvek registered trademark
- the sealing member 150 formed with the high density polyethylene nonwoven fabric becomes opaque.
- An adhesive application region 151 a and an adhesive non-application region 151 b are formed on the surface of the sealing member 150 facing the container body 140.
- a thermoplastic adhesive hot melt
- the adhesive application area 151 a comes into contact with the flange 143 of the container body 40. Thereafter, the contact portion between the sealing member 150 and the flange 143 is heated by the mold, whereby the adhesive is dissolved and the sealing member 150 and the flange 143 are heat-sealed (adhered).
- This adhesive non-application area 151b is set in an area facing a connection portion (one end face) 103 (described later) of the needle member 110 housed in the container main body 140.
- the needle member 110 shown in FIGS. 8 and 9 is attached to a syringe (such as a pen-type syringe) whose tip is sealed with a rubber stopper.
- the needle member 110 includes a double-ended needle 111 having needle tips at both ends, a needle holding portion 112 that holds an intermediate portion of the double-ended needle 111, and a connection portion 113 that is continuous with the needle holding portion 112.
- the needle holding portion 112 is formed in a substantially cylindrical shape and holds the middle portion of the double-ended needle 111.
- the connecting portion 113 is provided continuously at one end portion in the axial direction of the needle holding portion 112, and is formed in a substantially cylindrical shape having a cylindrical hole 113a.
- One end of the double-ended needle 111 is disposed in the connecting portion 113.
- the end surface of the connection portion 113 opposite to the needle holding portion 112 is the one end surface of the needle member 110, and the end surface of the needle holding portion 112 opposite to the connection portion 113 is the other end surface of the needle member 110.
- One end surface of the needle member 110 faces the sealing member 150. Further, the end surface of the connection portion 113 on the side of the needle holding portion 112 is in contact with the step portion 146 a of the container main body 140.
- a female thread portion 113b is formed on the inner peripheral surface of the connecting portion 113.
- the connecting portion 113 is screwed with the tip of a syringe whose tip is sealed with a rubber stopper. That is, a male screw portion that is screwed into the female screw portion 113b of the needle member 110 is provided at the distal end portion of the syringe.
- the needle tip formed at one end portion of the double-ended needle 111 is punctured by a rubber stopper that seals the distal end portion of the syringe.
- the double-ended needle 111 communicates with the internal space of the syringe.
- a cap member 120 is attached to the needle holding portion 112.
- the cap member 120 is formed in a substantially cylindrical shape, and one end in the axial direction is open and the other end in the axial direction is closed.
- the cap member 120 covers the other end portion of the double-ended needle 111 protruding from the needle holding portion 112. Further, the outer peripheral surface of the cap member 120 is provided with a protrusion 121 that engages with the inner surface of the tapered cylinder 147 in the container main body 140.
- the same effect as that of the syringe package of the first to third embodiments can be obtained. That is, when the sterilization process is performed on the needle member package 180, the sealing member 150 is pressed by high-temperature steam or gas and deformed so as to be recessed inside the container body 140. As a result, the surface of the sealing member 150 that faces the container body 140 abuts on the end surface of the connection portion 113 of the needle member 110.
- the region facing the connecting portion 113 side on the surface facing the container main body 140 of the sealing member 150 is the adhesive non-application region 151b where no adhesive is applied. Therefore, even if the surface of the sealing member 150 facing the container main body 140 abuts on the end surface of the connection part 113 in the needle member 110, the adhesive does not adhere to the connection part 113.
- the medical device package of the first to third embodiments described above is configured to store the syringe 10 which is a specific example of the medical device.
- the medical device package of the fourth embodiment is configured to house the needle member 110 which is another specific example of the medical device.
- a connector for connecting tubes, a syringe and a tube, or a drug container and a tube may be applied.
- the sealing member is manufactured by applying an adhesive to the portion of the nonwoven fabric where the adhesive is applied.
- the sealing member according to the present invention may be manufactured by bonding a nonwoven fabric formed in the size of the adhesive non-application area to a nonwoven fabric coated with an adhesive on the entire surface.
- two or more inner sheets 60 may be stacked and placed on the flange portion 16 of the syringe 10. In this case, even if the adhesive is applied to the entire surface of the sealing member facing the container body 40, the top or top to several inner sheets 60 are bonded to the sealing member. It will be. And the filling port 15 side of the several syringe 10 can be covered with the inner sheet 60 of several sheets from the bottom or the bottom.
- the medical device package is configured to include the inner sheet 60.
- the medical device package of the present invention may be configured not to include the inner sheet 60.
- the inner sheet 60 can be omitted.
- the adhesive non-application region 50b of the sealing member 50 is a region facing the plurality of syringes 10, and in the second embodiment described above, the bonding of the sealing member 51 is performed.
- the agent non-application area 51 b is an area facing the inner sheet 60.
- the adhesive non-application area 52b of the sealing member 52 is an area facing the opening 40a.
- region which concerns on this invention is not limited to these, What is necessary is just an area
- region which concerns on this invention you may set to the area
- the protrusion 45 serving as a bonding portion with the sealing member is provided on the flange 43 of the container body 40.
- the container main body according to the present invention may be one in which the protrusions 45 are not formed on the flange 43.
- the sealing member is heat-sealed (adhered) to the upper surface 43 a of the flange 43.
- the sealing member 50 having the adhesive application region 50a having a larger area than the flange 43 or the sealing member 51 having the adhesive application region 51a having a larger area than the flange 43 is sealed. It is good to apply as a stop member. Thereby, even if the sealing member 50 or 51 is displaced to some extent with respect to the container main body, the adhesive application region 50a or 51a can be brought into contact with the flange 43 of the container main body to bond them.
- the mounting shelf 44 is formed by making the longitudinal sectional shape of the peripheral wall portion 42 a crank shape.
- the mounting shelf according to the present invention may be, for example, a protruding portion that is continuous with the inner surface of the peripheral wall portion and protrudes substantially parallel to the bottom portion 41.
- the mounting shelf according to the present invention does not need to be continuous in the circumferential direction along the inner wall surface of the peripheral wall portion, and is provided discontinuously along the inner wall surface of the peripheral wall portion as long as the syringe holding member can be supported. Also good.
- the mounting shelf may be formed by a plurality of ribs that are continuous with the inner surface of the peripheral wall portion and the bottom portion 41 and protrude substantially parallel to the bottom portion 41.
- the container body 40 is formed in a box shape having an upper portion opened.
- the container body according to the present invention may be formed in a bottomed cylindrical shape, for example.
- the syringe storage container 1 that stores the syringe 10 with the needle and the syringe package 80 are described as examples.
- the medical device package of the present invention may contain a syringe to which a needle is not attached.
- the syringe holding member 30 of the above-described first to third embodiments holds the syringe 10 so that the filling port 15 faces upward (towards the upper end).
- a method for filling a syringe with a chemical solution (medicine) there is also a method for filling the drug solution (medicine) from a discharge portion of the syringe using a filling nozzle.
- the syringe is held by the syringe holding member so that the discharge portion faces upward (towards the upper end).
- the discharge part of the syringe also serves as a filling port for filling the chemical solution
- the discharge part side of the syringe is one end surface of the medical device according to the present invention.
- the sealing member formed in a quadrangle substantially equal to the contour of the outer periphery of the flange 43 is used.
- a sealing member formed in a long strip shape and wound and stored in a roll shape may be used.
- a large number of container bodies 40 on which the syringe holding member 30 holding the syringe 10 is placed are arranged.
- the sealing member is pulled out from the roll so as to cover the many container bodies 40 arranged, and placed on the ridges 45 of the many container bodies 40.
- the sealing member is heated and pressurized with a mold corresponding to the size of the drawn sealing member, and the protrusion 45 and the sealing member are heat-sealed using an adhesive.
- the syringe package 80 is assembled by cutting the sealing member along the contour of the outer periphery of the flange 43 in each container body 40.
- the present invention can be used for a medical device container for storing a medical device.
- SYMBOLS 1 ... Syringe storage container (medical device container), 10 ... Syringe (medical device), 11 ... Syringe main body, 12 ... Discharge part, 13 ... Needle tube, 15 ... Filling port, 16 ... Flange part, 20, 120 ... Cap member, 30 ... Syringe holding member (holding part) 31 ... Base plate 31a ... Through hole 32 ... Tube part 32a ... Tube hole 40, 140 ... Container body 41, 141 ... Bottom part 41a ... Inner surface 42, 142 ... peripheral wall, 43, 143 ... flange, 43a ... upper surface, 43b ... lower surface, 44 ... mounting shelf, 44a ... flat surface, 45 ... ridge, 45a ...
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Abstract
Description
容器本体は、上端部と下端部とを有する周壁部と、下端部に連続し、下端部に囲まれた底部と、上端部に囲まれた開口部と、周壁部と底部と開口部とから形成される収納空間と、収納空間内に設けられ、一端面が上端向きになるように医療用具を保持する保持部を有する。
封止部材は、容器本体に接着され、容器本体の開口部を封止する。この封止部材の容器本体に対向する面は、接着剤が塗布された接着剤塗布領域と、接着剤が塗布されていない接着剤非塗布領域を有している。そして、接着剤非塗布領域は、少なくとも保持部に保持された医療用具の一端面に対向する領域である。
また、医療用具と封止部材との間にインナーシート(保護シート)が配置されている場合は、封止部材がインナーシートに接触しても、インナーシートに接着剤が付着しない。
(1)
一端面と他端面とを有する医療用具と、前記医療用具を収納する医療用具収納容器とからなる医療用具梱包体であって、
前記医療用具収納容器は、
上端部と下端部とを有する周壁部と、前記下端部に連続し、前記下端部に囲まれた底部と、前記上端部に囲まれた開口部と、前記周壁部と前記底部と前記開口部とから形成される収納空間と、前記収納空間内に設けられ、前記一端面が上端向きになるように前記医療用具を保持する保持部を有する容器本体と、
前記容器本体に接着され、前記容器本体の前記開口部を封止するシート状の封止部材と、を備え、
前記封止部材の前記容器本体に対向する面は、接着剤が塗布された接着剤塗布領域と、接着剤が塗布されていない接着剤非塗布領域とを有し、前記接着剤非塗布領域は、少なくとも前記保持部に保持された前記医療用具の前記一端面に対向する領域である医療用具梱包体。
前記医療用具は、一端面と他端面とを有し、前記一端面に薬液を充填するための充填口が設けられたシリンジであり、
前記保持部は、前記周壁部の内面に係合して前記底部に対向し、前記シリンジの前記一端面が上端向きになるように前記シリンジを保持するシリンジ保持部材からなる(1)に記載の医療用具梱包体。
前記シリンジ保持部材に保持される前記シリンジの一端面側を覆うインナーシートを備える(2)に記載の医療用具梱包体。
前記接着剤非塗布領域は、少なくとも前記インナーシートに対向する領域である(3)に記載の医療用具梱包体。
前記接着剤非塗布領域は、少なくとも前記開口部に対向する領域である(1)~(4)のいずれかに記載の医療用具梱包体。
前記シリンジは、前記他端面を形成し、前記薬液を排出する排出部が設けられた(2)~(5)のいずれかに記載の医療用具梱包体。
前記容器本体は、前記上端部に連続し、前記上端部を囲むフランジ部を有し、
前記封止部材は、前記フランジ部に接着される(1)~(6)のいずれかに記載の医療用具梱包体。
前記封止部材は、熱を加えられた前記接着剤が融解することにより、前記容器本体に接着される(1)~(7)のいずれかに記載の医療用具梱包体。
前記容器本体に収納された前記医療用具は、前記封止部材を透過する高圧蒸気により、滅菌処理が施されている(1)~(8)のいずれかに記載の医療用具梱包体。
なお、説明は以下の順序で行う。
1.医療用具梱包体の第1の実施の形態
2.医療用具梱包体の第2の実施の形態
3.医療用具梱包体の第3の実施の形態
4.医療用具梱包体の第4の実施の形態
5.変形例
[医療用具梱包体の構成]
まず、第1の実施の形態に係る医療用具梱包体の構成について、図1及び図2を参照して説明する。
図1は、第1の実施の形態に係る医療用具梱包体の斜視図である。図2は、第1の実施の形態に係る医療用具梱包体の分解斜視図である。
シリンジ保持部材30は、本発明に係る保持部の一具体例を示すものであり、後述する充填口15を上向きにした状態のシリンジ10を保持する。このシリンジ保持部材30は、容器本体40の後述する載置棚44(図3参照)に載置され、容器本体40の後述する底部41に対向する。
インナーシート60は、四角形のシート状に形成されている。このインナーシート60の面積は、シリンジ保持部材30に保持されたシリンジ10の後述する充填口15側を覆う大きさに設定されている。インナーシート60は、シリンジ保持部材30に保持されたシリンジ10の後述するフランジ部16上に載置される。
次に、容器本体40について、図3を参照して説明する。
図3は、容器本体40の斜視図である。
次に、封止部材50について、図4を参照して説明する。
図4は、封止部材50の容器本体40と対向する面を上方に向けた状態の斜視図である。
次に、シリンジ10について、図5を参照して説明する。
図5は、シリンジ梱包体80の部分縦断面図である。
本実施の形態では、シリンジ本体11の充填口15側の端面を一端面とし、排出部12の端面を他端面とする。
なお、フランジ部16の形状は、本実施形態の楕円状に限られず、例えば、円環状であってもよい。
シリンジ10は、排出部12にキャップ部材20を装着した状態で、シリンジ保持部材30に設けられた貫通孔31aに挿入されて、シリンジ保持部材30に保持される。
次に、シリンジ梱包体80の組立方法について説明する。
[医療用具梱包体の構成]
次に、第2の実施の形態に係る医療用具梱包体の構成について、図6を参照して説明する。
図6は、第2の実施の形態に係る医療用具梱包体における封止部材の斜視図である。
図6に示す封止部材51は、容器本体40におけるフランジ43(図2参照)の外周の輪郭と略等しい四角形のシート状に形成されている。封止部材51は、容器本体40のフランジ43に接着剤を用いて熱融着される。具体的には、フランジ43の突条部45に熱融着される。この封止部材51が第1の実施の形態に係る封止部材50(図4参照)と異なるところは、接着剤塗布領域51aと接着剤非塗布領域51bである。
[医療用具梱包体の構成]
次に、第3の実施の形態に係る医療用具梱包体の構成について、図7を参照して説明する。
図7は、第3の実施の形態に係る医療用具梱包体における封止部材の斜視図である。
図7に示す封止部材52は、容器本体40におけるフランジ43(図2参照)の外周の輪郭と略等しい四角形のシート状に形成されている。封止部材52は、容器本体40のフランジ43に接着剤を用いて熱融着される。具体的には、フランジ43の突条部45に熱融着される。この封止部材52が第1の実施の形態に係る封止部材50(図4参照)と異なるところは、接着剤塗布領域52aと接着剤非塗布領域52bである。
[医療用具梱包体の構成]
次に、第4の実施の形態に係る医療用具梱包体の構成について、図8及び図9を参照して説明する。
図8は、第4の実施の形態に係る医療用具梱包体の縦断面図である。図9は、第4の実施の形態に係る医療用具梱包体の分解図である。
次に、容器本体140について説明する。
図8に示すように、容器本体140は、上端部と下端部とを有する周壁部142と、周壁部142の下端部に連続し、下端部に囲まれた底部141と、周壁部142の上端部に囲まれた開口部140aと、周壁部142の上端部に連続するフランジ143を有している。周壁部142と底部141と開口部140aに囲まれた容器本体140の内部空間は、針部材110を収納する収納空間となる。
次に、封止部材150について説明する。
図9に示すように、封止部材150は、シート状に形成されており、円形部150aと、円形部150の一部に連続する把持部150bを有している。円形部150aの外径は、容器本体140におけるフランジ143の外周の輪郭よりも少し大きく設定されている。封止部材150の円形部150aは、容器本体140のフランジ143に接着剤を用いて熱融着される。把持部150bは、一辺が円形部150bに連続する略三角形に形成されている。この把持部150bは、容器本体140に接着されない。
次に、針部材110について説明する。
図8及び図9に示す針部材110は、先端部がゴム栓で封止されたシリンジ(ペン型シリンジなど)に取り付けられる。この針部材110は、両端に針先を有する両頭針111と、この両頭針111の中間部を保持する針保持部112と、針保持部112に連続する接続部113を備えている。
以上、医療用具梱包体の実施の形態について、その作用効果も含めて説明した。しかしながら、本発明の医療用具梱包体は、上述しかつ図面に示した実施の形態に限定されるものではなく、特許請求の範囲に記載した発明の要旨を逸脱しない範囲内で種々の変形実施が可能である。
この場合は、封止部材の容器本体40に対向する面の全面に接着剤が塗布されていても、一番上又は一番上から数枚までのインナーシート60が封止部材に接着されることになる。そして、一番下又は一番下から数枚までのインナーシート60により複数のシリンジ10の充填口15側を覆うことができる。
本発明に係る接着剤非塗布領域としては、例えば、容器本体40のフランジ43に設けた突条部45の内周の輪郭よりも内側の部分に対向する領域に設定してもよい。つまり、接着剤塗布領域を突条部45に対向する領域に設定してもよい。この場合は、使用する接着剤の量を減らすことができるため、医療用具梱包体の製造に要するコストの削減を図ることができる。なお、この場合は、封止部材と容器本体を高精度に位置合せして、接着不良を回避する必要がある。
このような容器本体を用いる場合は、フランジ43よりも面積の大きい接着剤塗布領域50aを有する封止部材50、又はフランジ43よりも面積の大きい接着剤塗布領域51aを有する封止部材51を封止部材として適用するとよい。これにより、封止部材50又は51が容器本体に対してある程度ずれていても、接着剤塗布領域50a又は51aを容器本体のフランジ43に当接させて、両者を接着することができる。
また、本発明に係る載置棚は、周壁部の内壁面に沿って周方向に連続する必要な無く、シリンジ保持部材を支持できれば、周壁部の内壁面に沿って不連続に設けられていてもよい。この場合、載置棚は、周壁部の内面および底部41と連続し、底部41に対して略平行に突出する複数のリブにより形成されていてもよい。
この場合におけるシリンジ梱包体(医療用具梱包体)の組立方法としては、シリンジ10が保持されたシリンジ保持部材30を載置した容器本体40を多数並べる。次に、並べられた多数の容器本体40を覆う分だけロールから封止部材を引き出し、多数の容器本体40の突条部45に載せる。続いて、引き出した封止部材の大きさに対応した金型で、封止部材を加熱及び加圧して、突条部45と封止部材とを接着剤を用いて熱融着する。その後、各容器本体40におけるフランジ43の外周の輪郭に沿って、封止部材を切断することで、シリンジ梱包体80が組み立てられる。
Claims (9)
- 一端面と他端面とを有する医療用具と、前記医療用具を収納する医療用具収納容器とからなる医療用具梱包体であって、
前記医療用具収納容器は、
上端部と下端部とを有する周壁部と、前記下端部に連続し、前記下端部に囲まれた底部と、前記上端部に囲まれた開口部と、前記周壁部と前記底部と前記開口部とから形成される収納空間と、前記収納空間内に設けられ、前記一端面が上端向きになるように前記医療用具を保持する保持部を有する容器本体と、
前記容器本体に接着され、前記容器本体の前記開口部を封止するシート状の封止部材と、を備え、
前記封止部材の前記容器本体に対向する面は、接着剤が塗布された接着剤塗布領域と、接着剤が塗布されていない接着剤非塗布領域とを有し、前記接着剤非塗布領域は、少なくとも前記保持部に保持された前記医療用具の前記一端面に対向する領域である医療用具梱包体。 - 前記医療用具は、一端面と他端面とを有し、前記一端面に薬液を充填するための充填口が設けられたシリンジであり、
前記保持部は、前記周壁部の内面に係合して前記底部に対向し、前記シリンジの前記一端面が上端向きになるように前記シリンジを保持するシリンジ保持部材からなる請求項1に記載の医療用具梱包体。 - 前記シリンジ保持部材に保持される前記シリンジの一端面側を覆うインナーシートを備える請求項2に記載の医療用具梱包体。
- 前記接着剤非塗布領域は、少なくとも前記インナーシートに対向する領域である請求項3に記載の医療用具梱包体。
- 前記接着剤非塗布領域は、少なくとも前記開口部に対向する領域である請求項1に記載の医療用具梱包体。
- 前記シリンジは、前記他端面を形成し、前記薬液を排出する排出部が設けられた請求項2に記載の医療用具梱包体。
- 前記容器本体は、前記上端部に連続し、前記上端部を囲むフランジ部を有し、
前記封止部材は、前記フランジ部に接着される請求項1のいずれかに記載の医療用具梱包体。 - 前記封止部材は、熱を加えられた前記接着剤が融解することにより、前記容器本体に接着される請求項1に記載の医療用具梱包体。
- 前記容器本体に収納された前記医療用具は、前記封止部材を透過する高圧蒸気により、滅菌処理が施されている請求項1に記載の医療用具梱包体。
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WO2017170636A1 (ja) * | 2016-03-31 | 2017-10-05 | テルモ株式会社 | シリンジ保持部材、シリンジ梱包体及びシリンジ梱包体の組立方法 |
JPWO2017170636A1 (ja) * | 2016-03-31 | 2019-02-07 | テルモ株式会社 | シリンジ保持部材、シリンジ梱包体及びシリンジ梱包体の組立方法 |
EP3437621A4 (en) * | 2016-03-31 | 2019-10-09 | Terumo Kabushiki Kaisha | SYRINGE HOLDING MEMBER, SYRINGE ASSEMBLY BODY, AND METHOD OF ASSEMBLING SYRINGE ASSEMBLY BODY |
WO2019093351A1 (ja) * | 2017-11-10 | 2019-05-16 | テルモ株式会社 | 医療機器梱包体及びその製造方法 |
WO2021009890A1 (ja) | 2019-07-18 | 2021-01-21 | 株式会社大協精工 | 医療用機器コンテナー |
US11161671B2 (en) | 2019-07-18 | 2021-11-02 | Daikyo Seiko Ltd. | Medical device container |
KR20220035131A (ko) | 2019-07-18 | 2022-03-21 | 가부시끼가이샤 다이쿄 세이코 | 의료용 기기 컨테이너 |
Also Published As
Publication number | Publication date |
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JP6393738B2 (ja) | 2018-09-19 |
EP2818190B1 (en) | 2016-11-02 |
EP2818190A1 (en) | 2014-12-31 |
IN2014DN07800A (ja) | 2015-05-15 |
US20140353190A1 (en) | 2014-12-04 |
JP2017080478A (ja) | 2017-05-18 |
JP6072758B2 (ja) | 2017-02-01 |
US9925327B2 (en) | 2018-03-27 |
US20170189603A1 (en) | 2017-07-06 |
US9623171B2 (en) | 2017-04-18 |
CN110251766A (zh) | 2019-09-20 |
JPWO2013125443A1 (ja) | 2015-07-30 |
EP2818190A4 (en) | 2015-07-29 |
CN104159622A (zh) | 2014-11-19 |
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