InterDry 7912
InterDry 7912 is a Class I device made by Coloplast Corp., cleared under FDA 510(k) K110715 on 4 Nov 2011 and listed in FDA GUDID since 9 Apr 2021 (UDI-DI 00311701069525), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00311701069525 | Date9 Apr 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK110715 | Date4 Nov 2011 | StatusActive |
Official records
- AccessGUDID record 00311701069525
- FDA 510(k) database K110715
Across registries
- FDA 510(k) K110715 decided 4 Nov 2011 Active
- FDA GUDID UDI-DI 00311701069525 listed 9 Apr 2021 Listed
Timeline
- Cleared FDA 510(k) K110715
- Listed FDA GUDID 00311701069525
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- InterDry
- Generic name
- Antimicrobial skin friction/moisture control fabric, single-patient reusable
- Model / Ref / Catalog
- 7912
- Primary DI / UDI-DI
- 00311701069525
- 510(k) Number
- FDA product code
- FRL
- GMDN term
- Antimicrobial skin friction/moisture control fabric, single-patient reusable
- Device class
- Class I
- Regulation number
- 880.5300
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 10 InchLength — 36 Inch
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