PolyMem SportsWrap
by Ferris Mfg. Corp. 4 variants
Ref 9336
PolyMem SportsWrap (9336) is a Class I device made by Ferris Mfg. Corp., registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI 07354710184X) and listed in FDA GUDID since 31 Aug 2020 (UDI-DI 10735471093363), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number07354710184X 10735471093363 | Date14 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10735471093363 | Date31 Aug 2020 | StatusListed |
Official records
- EUDAMED public site 07354710184X
- AccessGUDID record 10735471093363
Across registries
- EUDAMED Basic UDI-DI 07354710184X registered 14 Sep 2026 Active
- FDA GUDID UDI-DI 10735471093363 listed 31 Aug 2020 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 10735471093363
- Registered EUDAMED 07354710184X
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- SportsWrap Roll Dressing EUDAMEDPolyMem GUDID
- Generic name
- Wound-nonadherent dressing, permeable, non-antimicrobial
- Model / Ref / Catalog
- 9336, SportsWrap
- Primary DI / UDI-DI
- 10735471093363
- Basic UDI-DI
- 07354710184X
- FDA product code
- IQI
- EMDN code
- M040204 Non-adherent absorbent dressings
- GMDN term
- Wound-nonadherent dressing, permeable, non-antimicrobial
- Device class
- Class I
- Regulation number
- 890.3475
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 9336 | SportsWrap |
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