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WO2025003015A1 - Emballage pour produit en forme de bande pour soins de plaie - Google Patents

Emballage pour produit en forme de bande pour soins de plaie Download PDF

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Publication number
WO2025003015A1
WO2025003015A1 PCT/EP2024/067516 EP2024067516W WO2025003015A1 WO 2025003015 A1 WO2025003015 A1 WO 2025003015A1 EP 2024067516 W EP2024067516 W EP 2024067516W WO 2025003015 A1 WO2025003015 A1 WO 2025003015A1
Authority
WO
WIPO (PCT)
Prior art keywords
chamber
shaped product
band
packaging
cover element
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
PCT/EP2024/067516
Other languages
German (de)
English (en)
Inventor
Thorsten GUTER
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Paul Hartmann AG
Original Assignee
Paul Hartmann AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Paul Hartmann AG filed Critical Paul Hartmann AG
Publication of WO2025003015A1 publication Critical patent/WO2025003015A1/fr
Pending legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/00051—Accessories for dressings
    • A61F13/00072—Packaging of dressings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F15/00—Auxiliary appliances for wound dressings; Dispensing containers for dressings or bandages
    • A61F15/001—Packages or dispensers for bandages, cotton balls, drapes, dressings, gauze, gowns, sheets, sponges, swabsticks or towels
    • 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
    • B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes or webs of flexible sheet material, e.g. in folded wrappers
    • B65D75/28—Articles or materials wholly enclosed in composite wrappers, i.e. wrappers formed by associating or interconnecting two or more sheets or blanks
    • B65D75/30—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding
    • B65D75/32—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents
    • B65D75/325—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet being recessed, and the other being a flat not- rigid sheet, e.g. puncturable or peelable foil
    • B65D75/327—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet being recessed, and the other being a flat not- rigid sheet, e.g. puncturable or peelable foil and forming several compartments
    • B65D75/328—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet being recessed, and the other being a flat not- rigid sheet, e.g. puncturable or peelable foil and forming several compartments the compartments being interconnected, e.g. by small channels
    • 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
    • B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes or webs of flexible sheet material, e.g. in folded wrappers
    • B65D75/52—Details
    • B65D75/58—Opening or contents-removing devices added or incorporated during package manufacture
    • B65D75/5855—Peelable seals

Definitions

  • the invention relates to a packaging for a band-shaped product for wound care, in particular a wound tamponade, a packaging containing a band-shaped product for wound care and a method for removing the band-shaped product.
  • band-shaped products for wound care are provided in sterile packaging with a length of at least 1 meter.
  • the medical staff cuts off the required length from the tamponade bandage in the packaging, soaks the severed piece of the tamponade bandage in a solution and inserts the tamponade into one nostril or ear canal.
  • the piece of the tamponade bandage still in the packaging is then pulled out of the packaging and used in the same way for the second nostril or ear canal.
  • Various types of packaging are known in the prior art, for example rigid polyethylene boxes that can be used as dispensers.
  • the strip-shaped product can be pulled out of the polyethylene box over the edge of a removal opening.
  • These polyethylene boxes are packed in additional sterile packaging so that they can be stored in a sterile condition. After the strip-shaped product has been removed, both the sterile packaging and the polyethylene box must be disposed of, which leads to disproportionately large amounts of waste.
  • sterile packaging so-called peel pouches, are used, which generate less waste but cannot be used as dispensers.
  • sterile packaging is described, for example, in EP 0 650 713 Bl.
  • the strip-shaped product is usually located between two layers of paper or film that are connected to one another at a peripheral edge, so that a chamber is formed within this edge in which the strip-shaped product can be accommodated.
  • a wound treatment kit is known from US 2010/ 0274205 Al.
  • the packaging has several individually sealed chambers, each chamber containing one component of the kit. On the
  • Cover of the chambers are instructions for the user, in which order the components of the kit should be taken out of the packaging and used.
  • the disadvantage of the known packaging is that the strip-shaped product always has to be pulled out over the edge of the packaging or the edge of the removal opening. Sterility in the edge area can only be inadequately ensured. In particular, if the product is removed multiple times, there is a risk that the edge will become dirty and the required cleanliness of the strip-shaped product can no longer be ensured.
  • the invention is therefore based on the object of proposing a packaging for a band-shaped product for wound care, by means of which the risk of soiling and/or contamination of the band-shaped product with germs during removal is reduced.
  • a packaging for a band-shaped product for wound care which comprises a molded element and a covering element, wherein the covering element is opposite the molded element and is at least partially connected to the molded element in a sealing zone.
  • a first chamber which is formed between the covering element and the molded element, is designed to receive the band-shaped product.
  • a second chamber, which is formed between the covering element and the Formed element is designed to receive an end section of the band-shaped product.
  • the packaging additionally comprises a connecting lumen between the first and the second chamber, wherein the end section of the band-shaped product can be passed through the connecting lumen from the first into the second chamber.
  • the design of the packaging has the advantage that the space formed between the cover element and the formed element, namely the first and second chambers and the connecting lumen, is protected from external contamination.
  • a band-shaped product stored in the first chamber of the packaging according to the invention can thus be guided out of the first chamber, through the connecting lumen, into the second chamber, without the band-shaped product having to be pulled over an unsterile or potentially contaminated edge of the packaging.
  • the second chamber can hold the strip-shaped product and can thus be used as a base or tray for placing the strip-shaped product. This means that no additional tray is required.
  • the risk of the section of the strip-shaped product pulled out of the first chamber falling onto the floor or a shelf and thus becoming dirty is reduced. For example, if the entire strip-shaped product is not required, but only a piece of it, the strip-shaped product can be pulled out of the first chamber and placed in the second chamber. The piece in the second chamber can then be severed from the remaining strip-shaped product without the severed piece having to be placed in an external container, such as a kidney dish.
  • the second chamber can also be used directly to apply ointments and solutions to the band-shaped product.
  • a section separated from the band-shaped product can be placed in the second chamber and then a solution containing active ingredients can be filled into the second chamber.
  • the soaked section is applied to the patient by the user, for example a doctor.
  • a further section of the band-shaped product can then be soaked in the second chamber.
  • the second chamber serves as a sterile base and storage for a section of the band-shaped product.
  • the first chamber together with the connecting lumen serves as a kind of dispenser from which the band-shaped product can be dispensed.
  • the sealing zone can run along an outer circumference of the packaging.
  • the cover element and the shaped element are not connected to one another at a side edge or corner of the packaging, so that the two elements can be lifted off freely there and pulled apart to open the packaging.
  • the cover element can have a larger area than the shaped element.
  • the cover element preferably protrudes beyond the shaped element on one side or corner of the packaging, so that a tab is formed. This tab enables the packaging to be opened more easily.
  • the cover element and the mold element can be joined in the sealing zone by any sealing method that results in an airtight seal in order to maintain the sterility of the tape-shaped product contained in the package.
  • the cover element and the mold element can be joined together by ultrasonic welding or gluing.
  • the elements are joined together by heat sealing.
  • a band-shaped product is understood to mean a product whose longitudinal extent is generally greater than the transverse extent.
  • a product can also be referred to as strip-shaped.
  • the band-shaped product is not rigid, but flexible and can therefore be rolled up.
  • the band-shaped product can be a gauze bandage or a gauze, as described for example in DIN EN 14079.
  • the packaging according to the invention is suitable for packaging a tamponade bandage or wound tamponade. Tamponade bandages are often not applied in one piece, but divided into sections.
  • the second chamber is particularly advantageous here, since the section already pulled out of the first chamber can be placed in the second chamber.
  • the band-shaped product can be accommodated in the first chamber in roll form.
  • This enables the band-shaped product to be unrolled evenly and thus makes it easier to remove the band-shaped product from the packaging.
  • compression of the band-shaped product at the bending points can be prevented by using a band-shaped product arranged in roll form.
  • the volume of the second chamber can be larger than the volume of the first chamber. This means that the strip-shaped product can be placed loosely in the second chamber. In addition, the larger volume of the second chamber allows it to hold sufficient liquid to soak the strip-shaped product. Alternatively, the volumes of the two chambers can be approximately the same.
  • the first chamber may have a volume of 5 cm 3 to 150 cm 3 , preferably 10 cm 3 to 45 cm 3 .
  • the second chamber may preferably have a volume of 30 cm 3 to 300 cm 3 .
  • the volumes of the chambers may also be adapted to the dimensions of the strip-shaped product.
  • the connecting lumen is formed between the molded element and the cover element.
  • the first chamber can be separated from the second chamber by a web.
  • the web is formed in the mold element and runs from one long side of the mold element to the opposite long side.
  • the web is formed such that its front surface is a shorter distance from the cover element than the bottom surface of the first or second chamber.
  • the front surface of the web is not connected to the cover element.
  • the connecting lumen is thus formed between the front surface of the web and the cover element.
  • the connecting lumen also serves to keep the opening between the first and second chambers as small as possible.
  • the connecting lumen or the opening between the first and second chambers should be large enough so that the band-shaped product can be pulled out of the first chamber without great resistance.
  • there must be little resistance between the side surfaces of the connecting lumen and the band-shaped product so that a section of the band-shaped product that has already been pulled out of the first chamber cannot slip back. This also prevents dirt from entering the first chamber.
  • the internal dimensions of the connecting lumen correspond at least to the thickness and the width of the band-shaped product. This prevents the section of the band-shaped product pulled out of the first chamber or the end section of the band-shaped product from slipping back and prevents dirt from penetrating the first chamber.
  • the packaging can be sterilized.
  • the packaging can particularly preferably be sterilized with ethylene oxide (EO). This can prevent yellowing of the ribbon-shaped product and produce a high degree of whiteness.
  • EO ethylene oxide
  • markings or instructions in the form of text or pictograms can be applied to the cover element. It is particularly advantageous if the markings or instructions are printed on the cover element.
  • a marking line can be provided on the cover element, which is arranged such that it runs over the connecting lumen between the first and the second chamber, in particular over the web.
  • the marking line shows the user the limit up to which he can detach the cover element from the shaped element if he wants to open the packaging. If the cover element is only detachable up to the marking line, the second chamber is opened, but the first chamber remains closed by the cover element so that neither the band-shaped product can fall out nor the band-shaped product in the first chamber can become dirty. In addition, the user is prevented from touching the band-shaped product stored in the first chamber.
  • markings can be provided on the shaped element in the same way.
  • the cover element can have a groove or weakening that runs above the web and parallel to the web. This enables the cover element to be folded over in a pulling-on direction such that the area of the cover element that covers the second chamber comes to lie above the first chamber. This simplifies handling of the packaging and removal of the strip-shaped product.
  • the cover element can have a groove or weakening that runs above the web and parallel to the web. This enables the cover element to be folded over in a pulling-on direction such that the area of the cover element that covers the second chamber comes to lie above the first chamber. This simplifies handling of the packaging and removal of the strip-shaped product.
  • the cover element can be designed in two parts. One part of the cover element covers the first chamber and a second part of the cover element covers the second chamber. This embodiment also makes it possible to open the second chamber without removing the cover element above the first chamber.
  • the packaging preferably has a length of 5 cm to 20 cm and particularly preferably of 10 cm to 18 cm.
  • the width of the packaging is preferably between 4 cm and 10 cm. A width of 5 cm to 7 cm is particularly preferred.
  • the height of the packaging can be approximately the same as the width of the strip-shaped product, but can preferably be slightly larger.
  • the dimensions of the packaging are designed so that the user can hold the packaging between the fingers in one hand and open it with the other hand. This allows for particularly easy handling when using the packaging.
  • the cover element can be a foil made of metal or plastic, in particular a polyethylene foil. Particularly preferred is The cover element is made of paper or contains paper. This creates a
  • Preferred materials for the cover element are also nonwovens, in particular nonwovens made of high-density polyethylene (e.g. Tyvek, a registered trademark of DuPont) and other materials that provide a sufficiently large gas exchange surface to enable sterilization with ethylene oxide.
  • high-density polyethylene e.g. Tyvek, a registered trademark of DuPont
  • the molded element can consist of a plastic, preferably a thermoplastic and in particular a deep-drawable plastic.
  • a plastic preferably a thermoplastic and in particular a deep-drawable plastic.
  • suitable plastics are polypropylene (PP), polyamides (PA) and polyurethanes (PU), particularly preferred are polyethylene terephthalate (PET), amorphous polyethylene terephthalate, polyethylene (PE) and combinations thereof, such as PET/PE.
  • the mould element made of thermoformable plastic not only reduces the manufacturing costs, but also allows the volumes of the first and second chambers to be adjusted via the depth of the chambers. This allows the packaging to be different strip-shaped products can be adapted without the need to manufacture costly molds.
  • the molded element is formed in one piece, which enables a cost-effective and simple provision of the molded element and thus of the packaging.
  • kits which comprises a packaging according to one of the previously described embodiments and also a band-shaped product for wound care.
  • the band-shaped product is accommodated in the first chamber, with an end section of the band-shaped product being accommodated in the second chamber.
  • the end section of the band-shaped product is guided from the first chamber into the second chamber through the connecting lumen between the first and the second chamber.
  • the band-shaped product has a length of 0.2 m to 10 m, preferably of 0.5 m and 5 m and particularly preferably of 1 m to 2 m. This allows a suitable amount of the band-shaped product to be provided for the treatment of an individual patient. Furthermore, it is preferably provided that the width of the strip-shaped product is between 0.5 cm and 10 cm, preferably between 0.75 cm and 5 cm and particularly preferably between 1 cm and 2 cm. These are usual ranges for strip-shaped products.
  • the end portion of the ribbon-shaped product extends between 0.5 cm and 10 cm into the second chamber, preferably between 4 cm and 6 cm. This allows easy gripping with tweezers or fingers to pull the ribbon-shaped product out of the first chamber.
  • the end section is a free-standing end of the strip-shaped product.
  • the object is achieved by a method for removing the band-shaped product from a packaging according to one of the preceding embodiments.
  • the method comprises the following steps: a) partially detaching the cover element so that the second chamber is exposed and the first chamber remains covered by the cover element, b) grasping (for example with the hand or tweezers) the end section and pulling out a section of the band-shaped product from the first chamber, c) optionally separating the section from the strip-shaped product, d) positioning the section in the second chamber, and e) removing the section from the second chamber.
  • the method according to the invention enables a hygienic and ideally aseptic removal of the band-shaped product.
  • the band-shaped product does not have to be pulled out of a dispenser via a potentially contaminated edge, but is dispensed via the connecting lumen, which is located between the first and second chamber and is therefore sterile until the packaging is opened.
  • Aseptic is understood here as the reduction of contamination caused by harmful pathogenic microorganisms such as bacteria or viruses.
  • step e the section in the second chamber is soaked with a treatment solution.
  • the soaked section is then removed from the second chamber and can be applied.
  • This offers the advantage that no further container has to be provided for soaking, but the packaging can be used directly. This means that a container is always available for soaking, namely the second chamber of the packaging. This also saves waste and costs.
  • the treatment solution can be, for example, saline solution, Ringer's solution or solutions containing antibiotics or disinfectants.
  • treatment solution also includes ointment-like compositions.
  • Other examples of a treatment solution are decongestant nasal drops, preparations containing myrtol or secretolytics.
  • a second section can be pulled out of the first chamber to also be soaked in the treatment solution already in the second chamber.
  • the treatment solution can be removed from the second chamber and then the steps of the method can be repeated from step b).
  • the web may preferably have a height of 1 mm to 10 mm, particularly preferably 5 mm.
  • Figure 1 shows a schematic section through an inventive
  • FIG. 1 is a perspective view of the packaging with inserted ribbon-shaped product
  • Figure 3 is a schematic representation of the first steps of the process for removing the strip-shaped product
  • Figure 4 is a schematic representation of further steps of the method for removing the strip-shaped product.
  • Figure 5 is a schematic representation of a further step of the method for removing the strip-shaped product.
  • FIG. 1 shows a schematic section through a package 10 in a first embodiment of the invention.
  • a deep-drawn molded element 11 is shaped in such a way that it forms a first chamber 14 and a second chamber 15, which are separated by a web 17.
  • a cover element 12 made of paper, which is suitable for medical purposes, is connected, in particular sealed, to the molded element 11 in a sealing zone 13, so that the first chamber 14 and the second chamber 15 are hermetically enclosed by the molded element 11 and the cover element 12.
  • the sealing zone 13 is designed in the figures as a peripheral edge of the package 10. In the area of the web 17, the cover element 12 is not connected to the molded element 11. so that the first chamber 14 is connected to the second chamber 15 via a
  • the molded element 11 is deep-drawn from a PET/PE film and is thus transparent. This allows the packaging
  • the thickness of the mold element 11 is approximately 350 pm, with the layer thickness of PET being approximately 300 pm and the layer thickness of PE being approximately 50 pm. A thickness of the mold element 11 of approximately 300 pm is also possible.
  • the packaging 10 preferably has a width of 7 cm and a length of 17.5 cm.
  • a band-shaped product 20 which is wound up in a roll shape, is inserted into the first chamber 14.
  • the cover element 12 is almost completely separated from the mold element 11, only in a section of the sealing zone 13 are the cover element 12 and the mold element
  • the cover element is only separated from the molded element 11 up to the level of the web 17, so that the second chamber 15 is opened, but not the first chamber 14.
  • An end section 21 of the band-shaped product 20 is guided through the connecting lumen 16 and thus over the web 17 from the first chamber 14 into the second chamber 15, so that this free-standing end of the band-shaped product 20 extends into the second chamber 15.
  • the second chamber 15 is larger than the first chamber 14 in order to enable easy removal of the strip-shaped product 20. This also allows the strip-shaped product 20 or a section thereof to be soaked with a treatment solution in the second chamber 15.
  • Figure 3 shows schematically the first steps of the method for removing the strip-shaped product 20 from the packaging 10.
  • the packaging 10 has dimensions that allow the packaging 10 to be easily held by the user in one hand. With the other hand, the user can then pull the cover element 12 off the molded element 11 starting at a corner near the second chamber 15 until the second chamber 15 is exposed. This means that the connection between the molded element 11 and the cover element 12 is separated in the sealing zone, up to the area of the connecting lumen 16. This area is indicated by a marking line (not shown) on the cover element 12. Alternatively or additionally, the molded element 11 can also have a groove that defines this area.
  • the web 17 can also be shaped in such a way that the
  • the end section 21 can then be grasped using tweezers or with the fingers and the strip-shaped product 20 can be pulled out of the first chamber 14 to the desired length.
  • the end section 21 and the strip-shaped product 20 pulled out of the first chamber 14 remain positioned within or at least substantially above the second chamber 15 so that it can be placed in the second chamber 15 and the strip-shaped product 20 is thus not soiled and/or contaminated with germs.
  • the band-shaped product 20 pulled out of the first chamber 14 and lying in the second chamber 15 can be severed, for example with scissors, from the band-shaped product 20 still in the first chamber 14, as shown in Figure 4. This is preferably done within the second chamber 15 so that a new end section 22 is created, from which a piece of the band-shaped product 20 can be pulled out again.
  • the separated piece of the band-shaped product 20 can now either be soaked with a treatment solution which is filled into the second chamber 15 or can be removed directly and applied. The treatment solution is preferably then removed from the second chamber 15.

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biomedical Technology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • Surgery (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Molecular Biology (AREA)
  • Medical Informatics (AREA)
  • Composite Materials (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Packages (AREA)

Abstract

L'invention concerne un emballage pour un produit en forme de bande pour le soin des plaies, comprenant : un élément façonné ; un élément de couvercle, qui se trouve à l'opposé de l'élément façonné et qui est relié au moins en partie à l'élément façonné dans une zone d'étanchéité ; une première chambre, qui est formée entre l'élément de couvercle et l'élément façonné, la première chambre étant conçue pour recevoir le produit en forme de bande ; une seconde chambre, qui est formée entre l'élément de couvercle et l'élément façonné, la seconde chambre étant conçue pour recevoir une partie d'extrémité du produit en forme de bande ; et une lumière de raccordement entre la première chambre et la seconde chambre, la partie d'extrémité du produit en forme de bande pouvant être guidée à travers la lumière de raccordement dans la seconde chambre. Cette invention se rapporte en outre à un kit et à un procédé.
PCT/EP2024/067516 2023-06-30 2024-06-21 Emballage pour produit en forme de bande pour soins de plaie Pending WO2025003015A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102023117315.4 2023-06-30
DE102023117315.4A DE102023117315A1 (de) 2023-06-30 2023-06-30 Verpackung für ein bandförmiges Produkt zur Wundpflege

Publications (1)

Publication Number Publication Date
WO2025003015A1 true WO2025003015A1 (fr) 2025-01-02

Family

ID=91758701

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2024/067516 Pending WO2025003015A1 (fr) 2023-06-30 2024-06-21 Emballage pour produit en forme de bande pour soins de plaie

Country Status (2)

Country Link
DE (1) DE102023117315A1 (fr)
WO (1) WO2025003015A1 (fr)

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WO1998038954A2 (fr) * 1997-03-06 1998-09-11 Surgi International (Proprietary) Limited Emballage resistant a l'eclatement
EP0650713B1 (fr) 1993-11-01 1999-09-15 Paul Hartmann Aktiengesellschaft Pansement et son emballage
US20100274205A1 (en) 2009-04-24 2010-10-28 Morelli Rocco R Wound care kit

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US5511689A (en) 1993-12-28 1996-04-30 Frank; Richard D. Dispensing device for adhesive-backed articles
DE19843963A1 (de) 1998-09-24 2000-03-30 Rauscher & Co Tampon und Tampon-Packung
ES2381422T3 (es) 2009-05-30 2012-05-28 Bayer Innovation Gmbh Producto con materiales de soporte biorreabsorbibles y envase
US20120211507A1 (en) 2011-02-18 2012-08-23 C. B. Medical, Inc. Dispenser System and Method
WO2015188225A1 (fr) 2014-06-10 2015-12-17 M4 Medical Pty Ltd Pansement
EP3473227A1 (fr) 2017-10-17 2019-04-24 Klinikum rechts der Isar der Technischen Universität München Dispositifs de manipulation des toiles à appliquer à un lieu d'utilisation

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EP0650713B1 (fr) 1993-11-01 1999-09-15 Paul Hartmann Aktiengesellschaft Pansement et son emballage
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US20100274205A1 (en) 2009-04-24 2010-10-28 Morelli Rocco R Wound care kit

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