DK1606196T4 - Damphydrering i en hydrofil kateteremballage - Google Patents
Damphydrering i en hydrofil kateteremballage Download PDFInfo
- Publication number
- DK1606196T4 DK1606196T4 DK04780281.4T DK04780281T DK1606196T4 DK 1606196 T4 DK1606196 T4 DK 1606196T4 DK 04780281 T DK04780281 T DK 04780281T DK 1606196 T4 DK1606196 T4 DK 1606196T4
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- DK
- Denmark
- Prior art keywords
- catheter
- liquid
- vapor
- catheter assembly
- package
- Prior art date
Links
- 230000036571 hydration Effects 0.000 title claims abstract description 34
- 238000006703 hydration reaction Methods 0.000 title claims abstract description 34
- 239000007788 liquid Substances 0.000 claims abstract description 172
- 238000000576 coating method Methods 0.000 claims abstract description 62
- 239000011248 coating agent Substances 0.000 claims abstract description 61
- 230000014759 maintenance of location Effects 0.000 claims abstract description 61
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 158
- 239000004744 fabric Substances 0.000 claims description 46
- 239000000463 material Substances 0.000 claims description 46
- 239000006260 foam Substances 0.000 claims description 32
- 238000003780 insertion Methods 0.000 claims description 27
- 230000037431 insertion Effects 0.000 claims description 27
- 239000000017 hydrogel Substances 0.000 claims description 12
- -1 polyethylene Polymers 0.000 claims description 12
- 210000002700 urine Anatomy 0.000 claims description 11
- 239000004698 Polyethylene Substances 0.000 claims description 10
- 238000004806 packaging method and process Methods 0.000 claims description 10
- 229920000573 polyethylene Polymers 0.000 claims description 10
- 239000011888 foil Substances 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 229920001410 Microfiber Polymers 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 239000003658 microfiber Substances 0.000 claims description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 229920001400 block copolymer Polymers 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- 239000004814 polyurethane Substances 0.000 claims description 3
- 210000003708 urethra Anatomy 0.000 claims description 3
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 238000013459 approach Methods 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims description 2
- 239000002985 plastic film Substances 0.000 claims description 2
- 229920006255 plastic film Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 230000008016 vaporization Effects 0.000 claims 12
- 230000000717 retained effect Effects 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 13
- 230000004913 activation Effects 0.000 abstract description 8
- 230000003111 delayed effect Effects 0.000 abstract description 2
- 238000012360 testing method Methods 0.000 description 35
- 239000010408 film Substances 0.000 description 25
- 239000000047 product Substances 0.000 description 21
- 230000032683 aging Effects 0.000 description 18
- 239000000499 gel Substances 0.000 description 13
- 230000008901 benefit Effects 0.000 description 10
- 230000000887 hydrating effect Effects 0.000 description 9
- 229920001971 elastomer Polymers 0.000 description 8
- 239000000806 elastomer Substances 0.000 description 8
- 230000005660 hydrophilic surface Effects 0.000 description 7
- 238000007654 immersion Methods 0.000 description 7
- 230000008961 swelling Effects 0.000 description 5
- 230000004888 barrier function Effects 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 3
- 239000006261 foam material Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 238000012858 packaging process Methods 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
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- 238000011109 contamination Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000012414 sterilization procedure Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
Classifications
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/002—Packages specially adapted therefor ; catheter kit packages
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/0009—Making of catheters or other medical or surgical tubes
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/0017—Catheters; Hollow probes specially adapted for long-term hygiene care, e.g. urethral or indwelling catheters to prevent infections
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
- A61M25/0111—Aseptic insertion devices
-
- 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
- B65B5/00—Packaging individual articles in containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, jars
- B65B5/04—Packaging single articles
-
- 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
- B65B55/22—Immersing contents in protective liquids
-
- 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
- B65B7/02—Closing containers or receptacles deformed by, or taking-up shape, of, contents, e.g. bags, sacks
-
- 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
- B65D81/00—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
- B65D81/18—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents providing specific environment for contents, e.g. temperature above or below ambient
- B65D81/22—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents providing specific environment for contents, e.g. temperature above or below ambient in moist conditions or immersed in liquids
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/0043—Catheters; Hollow probes characterised by structural features
- A61M25/0045—Catheters; Hollow probes characterised by structural features multi-layered, e.g. coated
- A61M2025/0046—Coatings for improving slidability
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/06—Body-piercing guide needles or the like
- A61M25/0662—Guide tubes
- A61M2025/0681—Systems with catheter and outer tubing, e.g. sheath, sleeve or guide tube
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0068—Static characteristics of the catheter tip, e.g. shape, atraumatic tip, curved tip or tip structure
- A61M25/007—Side holes, e.g. their profiles or arrangements; Provisions to keep side holes unblocked
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Animal Behavior & Ethology (AREA)
- Biophysics (AREA)
- Public Health (AREA)
- Pulmonology (AREA)
- Mechanical Engineering (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Media Introduction/Drainage Providing Device (AREA)
- External Artificial Organs (AREA)
- Materials For Medical Uses (AREA)
- Packages (AREA)
- Wrappers (AREA)
- Absorbent Articles And Supports Therefor (AREA)
Claims (21)
1. Brugsklar hydrofil katetersamling (10,110, 310, 410, 510, 610, 710, 810), som omfatter: en gasimpermeabel emballage (12, 312, 412, 512, 812), som har et forseglet hulrum, et hydrofilt coatet kateter (10, 110, 310, 410, 510, 610, 710, 810), som er anbragt inde i det forseglede hulrum, idet det hydrofile coatede kateter (10, 110, 310, 410, 510, 610, 710, 810) omfatter et rør (14, 114, 314, 414, 514, 614, 714, 814), som haren ydre overflade med en hydrofil coating på i det mindste en del deraf, som skal indsættes i urinrøret; en mængde væske anbragt inde i det forseglede hulrum; kendetegnet ved, at katetersamlingen desuden omfatter en indføringsspids (16, 316, 616, 716) ved en proksimal indsættelsesende af røret (14, 114, 314, 414, 514, 614, 714, 814), og et fleksibelt hylster (20,120, 320, 720), som er udformet af et damppermeabelt materiale, der er fastgjort til indføringsspidsen (16, 316, 616, 716) og strækker sig derfra til en distal ende af røret (14, 114, 314, 414, 514, 614, 714, 814); og hvor den brugsklare tilstand af kateret skyldes den dampgivende væske, som frembringer en dampatmosfære inde i den gasimpermeable emballage (12), som aktiverer det hydrofile coatede kateter.
2. Katetersamling ifølge krav 1, hvor den gasimpermeable emballage (12, 312, 412, 512,812) er udformet af et materiale, som har en impermeabilitet, der er tilstrækkelig til en lagerholdbarhed for produktet på mellem seks måneder og fem år.
3. Katetersamling ifølge krav 1, hvor den gasimpermeable emballage (12, 312, 412, 512, 812) er udformet af aluminiumfolie.
4. Katetersamling ifølge krav 1, hvor det hydrofile coatede kateter (10, 110, 310, 410, 510, 610, 710, 810) desuden omfatter drænhuller (18, 118, 318, 718), som er udformet i røret (14, 114, 314, 414, 514, 614, 714, 814) nærved en proksimal indsættelsesende deraf, og et forbindelsesstykke (22, 122, 522, 622, 722) ved en distal ende deraf.
5. Katetersamling ifølge krav 4, hvor forbindelsesstykket (22, 122, 522, 622, 722) omfatter en tilspidset tragt, som er integreret forbundet med den distale ende af røret (14, 114, 314, 414, 514, 614, 714, 814) til forbindelse med en indretning til opsamling af urin, der passerer gennem røret (14, 114, 314, 414, 514, 614, 714, 814).
6. Katetersamling ifølge krav 1, som omfatter indføringsspidsen (16, 316, 616, 716) ved en proksimal indsættelsesende af røret (14, 114, 314, 414, 514, 614, 714, 814), som har slidser til at definere flige, der bøjer udad for at danne en åbning til indføring af røret (14, 114, 314, 414, 514, 614, 714, 814) derigennem.
7. Katetersamling ifølge krav 5, som omfatter det fleksible hylster (20, 120, 320, 720), der er udformet af et damppermeabelt materiale, som er fastgjort til den tilspidsede tragt (22, 122, 522, 622, 722) og strækker sig, således at det dækker den proksimale indsættelsesende af røret (14, 114, 314, 414, 514, 614, 714, 814).
8. Katetersamling ifølge krav 1, hvor hylsteret (20, 120, 320, 720) er udformet af et damppermeabelt, væskeimpermeabelt sammenklappeligt polymert filmmateriale, som tætsiddende omgiver røret eller skaftet.
9. Katetersamling ifølge krav 1, hvor hylsteret (20, 120, 320, 720) er udformet af et materiale, som er valgt blandt polyethylen, blødgjort PVC, polypropylen, polyurethan og polyethylenoxid-blokcopolymer.
10. Katetersamling ifølge krav 9, hvor det polymere filmmateriale er Medifilm 435-poly-ethylenoxid-blokcopolymer med en tykkelse inden for området mellem 10 og 150 mikron.
11. Katetersamling ifølge krav 1, hvor den dampgivende væske er vand, som ikke omfatter mere end 20% af volumenet af det forseglede hulrum af emballagen (12, 312, 412, 512, 812).
12. Katetersamling ifølge krav 11, hvor vandet er mellem 2 og 5 ml, som ikke omfatter mere end 5% af volumenet af det forseglede hulrum af emballagen (12, 312, 412, 512, 812).
13. Katetersamling ifølge krav 1, hvor væsken holdes tilbage af et væskesekvestre-ringselement (330, 530, 630, 830) for at minimere risikoen for udslip, mens der frigives en damp til at frembringe dampatmosfæren inde i den gasimpermeable emballage (12, 312, 412, 512, 812), således at kateterets brugsklare tilstand skyldes den damp, der aktiverer i det mindste en del af det hydrofile coatede kateter for at sikre afgivelse af det hydrofile coatede kateter til brugeren i en fuldstændigt brugsklar tilstand.
14. Katetersamling ifølge krav 13, hvor det hydrofile coatede kateter, væsken og væ-skesekvestreringselementet (330, 530, 630, 830) er indeholdt inde i det forseglede hulrum af den gasimpermeable emballage (12, 312, 412, 512, 812), og væskesekvestre-ringselementetet (330, 530, 630, 830) omfatter et materiale til at absorbere den dampgivende væske.
15. Katetersamling ifølge krav 14, hvor materialet til at absorbere den dampgivende væske er et stof eller skum, som er i stand til at absorbere i det væsentlige al tilgængelig dampgivende væske og derefter frigive en damp fra den dampgivende væske for at frembringe og opretholde en fuldt mættet dampatmosfære i en ligevægtstilstand inde i det forseglede hulrum.
16. Katetersamling ifølge krav 15, hvor det hydrofile coatede kateter omfatter et rør (14, 114, 314, 414, 514, 614, 714, 814), som har en ydre overflade med den hydrofile coating på i det mindste en del deraf, og stoffet eller skummet i det væsentlige udstrækker sig sammen med og langs med røret (14, 114, 314, 414, 514, 614, 714, 814) inde i det forseglede hulrum for at frigive dampen tæt ved røret til optagelse af den hydrofile coating.
17. Katetersamling ifølge krav 16, hvor stoffet eller skummet er løst anbragt inde i det forseglede hulrum og er dimensioneret til at indeholde en tilstrækkelig mængde af den dampgivende væske til at opretholde en fuldt mættet dampatmosfære inde i det forseglede hulrum for at sikre kontinuerlig hydrering af det hydrofile coatede kateter i en acceptabel lagerholdbarhedstid for produktet.
18. Katetersamling ifølge krav 16, hvor stoffet eller skummet er fast anbragt inde i det forseglede hulrum og er dimensioneret til at indeholde en tilstrækkelig mængde af den dampgivende væske til at opretholde en fuldt mættet dampatmosfære inde i det forseg lede hulrum for at sikre kontinuerlig hydrering af det hydrofile coatede kateter i en acceptabel lagerholdbarhedstid for produktet.
19. Katetersamling ifølge krav 16, hvor materialet til at absorbere den dampgivende væske har mellemrum til at holde den dampgivende væske og frigive en damp derfra og har en overflade, som vender indad i det forseglede hulrum, og som tillader afgivelse af dampen, mens den samtidigt forhindrer materialet i at klæbe til det hydrofile kateter.
20. Katetersamling ifølge krav 19, hvor materialet omfatter et smelteblæst mikrofiber-stof, som har et højt kapillært træk af den dampgivende væske, og overfladen er dækket med et materiale, som er valgt blandt en tynd elastomer hydrogelfilm, et polymert netmateriale og en perforeret plastfilm.
21. Katetersamling ifølge krav 20, hvor materialet omfatter et smelteblæst mikrofiber-stof, som har et højt kapillært træk af den dampgivende væske, og overfladen er behandlet med henblik på at få det smelteblæste mikrofiberstof til at kunne fugtes med den dampgivende væske.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49349303P | 2003-08-08 | 2003-08-08 | |
| PCT/US2004/025417 WO2005014055A2 (en) | 2003-08-08 | 2004-08-06 | Vapor hydration in a hydrophilic catheter package |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DK1606196T3 DK1606196T3 (da) | 2012-07-02 |
| DK1606196T4 true DK1606196T4 (da) | 2016-04-04 |
Family
ID=34135250
Family Applications (7)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK17205430.6T DK3392167T3 (da) | 2003-08-08 | 2004-08-06 | Hydrofilt kateter i en emballage |
| DK04780281.4T DK1606196T4 (da) | 2003-08-08 | 2004-08-06 | Damphydrering i en hydrofil kateteremballage |
| DK11175016.2T DK2423126T4 (da) | 2003-08-08 | 2004-08-06 | Damphydrering af et hydrofilt kateter i en emballage |
| DK11175010.5T DK2423125T4 (da) | 2003-08-08 | 2004-08-06 | Damphydrering af hydrofilt kateter i en pakning |
| DK11175017.0T DK2423127T4 (da) | 2003-08-08 | 2004-08-06 | Damphydratisering af et hydrofilt kateter i en emballage |
| DK17150789.0T DK3210909T3 (da) | 2003-08-08 | 2004-08-06 | Hydrofilt kateter i en pakning |
| DKBA201300115U DK201300115U3 (da) | 2003-08-08 | 2013-07-30 | Damphydrering af et hydrofilt kateter i en emballage |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK17205430.6T DK3392167T3 (da) | 2003-08-08 | 2004-08-06 | Hydrofilt kateter i en emballage |
Family Applications After (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK11175016.2T DK2423126T4 (da) | 2003-08-08 | 2004-08-06 | Damphydrering af et hydrofilt kateter i en emballage |
| DK11175010.5T DK2423125T4 (da) | 2003-08-08 | 2004-08-06 | Damphydrering af hydrofilt kateter i en pakning |
| DK11175017.0T DK2423127T4 (da) | 2003-08-08 | 2004-08-06 | Damphydratisering af et hydrofilt kateter i en emballage |
| DK17150789.0T DK3210909T3 (da) | 2003-08-08 | 2004-08-06 | Hydrofilt kateter i en pakning |
| DKBA201300115U DK201300115U3 (da) | 2003-08-08 | 2013-07-30 | Damphydrering af et hydrofilt kateter i en emballage |
Country Status (12)
| Country | Link |
|---|---|
| US (9) | US7380658B2 (da) |
| EP (7) | EP2423127B2 (da) |
| JP (2) | JP4682135B2 (da) |
| AT (1) | ATE549056T1 (da) |
| AU (1) | AU2004263129B2 (da) |
| DE (3) | DE11175010T1 (da) |
| DK (7) | DK3392167T3 (da) |
| ES (6) | ES2578509T5 (da) |
| FI (1) | FI2423125T4 (da) |
| HU (4) | HUE053032T2 (da) |
| TR (1) | TR201808596T4 (da) |
| WO (1) | WO2005014055A2 (da) |
Families Citing this family (143)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7682353B2 (en) * | 2001-06-29 | 2010-03-23 | Coloplast A/S | Catheter device |
| US7517343B2 (en) * | 2001-06-29 | 2009-04-14 | Coloplast A/S | Catheter assembly |
| ES2320205T3 (es) * | 2001-06-29 | 2009-05-20 | Coloplast A/S | Un conjunto de cateter. |
| US8932262B2 (en) * | 2002-02-14 | 2015-01-13 | Ishay Ostfeld | Indwelling device |
| US20050085775A1 (en) * | 2002-02-14 | 2005-04-21 | Ishay Ostfeld | Indwelling device |
| FI2423125T4 (fi) | 2003-08-08 | 2024-11-28 | Hollister Inc | Hydrofiilisen katetrin höyryhydratointi pakkauksessa |
| US20060160373A1 (en) * | 2005-01-14 | 2006-07-20 | Cabot Corporation | Processes for planarizing substrates and encapsulating printable electronic features |
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2004
- 2004-08-06 FI FIEP11175010.5T patent/FI2423125T4/fi active
- 2004-08-06 DE DE11175010.5T patent/DE11175010T1/de active Pending
- 2004-08-06 ES ES11175016T patent/ES2578509T5/es not_active Expired - Lifetime
- 2004-08-06 HU HUE17205430A patent/HUE053032T2/hu unknown
- 2004-08-06 DE DE11175017.0T patent/DE11175017T1/de active Pending
- 2004-08-06 EP EP11175017.0A patent/EP2423127B2/en not_active Expired - Lifetime
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- 2004-08-06 HU HUE11175010A patent/HUE046203T2/hu unknown
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- 2004-08-06 ES ES04780281.4T patent/ES2384172T5/es not_active Expired - Lifetime
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- 2004-08-06 EP EP04780281.4A patent/EP1606196B2/en not_active Expired - Lifetime
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