Solventum™ 9668L
Ref 9668L
Solventum 9668L is a device of GMDN type surgical hair clippers (EU MDR Class I; FDA Class I; FDA product code LWK, Razor, Surgical) made by Solventum US LLC, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 01979988401010000000050MJ) and listed in FDA GUDID since 15 Feb 2026 (UDI-DI 00197998192715), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number01979988401010000000050MJ 00197998192715 | Date4 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00197998192715 | Date15 Feb 2026 | StatusListed |
Official records
- EUDAMED public site 01979988401010000000050MJ
- AccessGUDID record 00197998192715
Across registries
- EUDAMED Basic UDI-DI 01979988401010000000050MJ registered 4 Nov 2026 Active
- FDA GUDID UDI-DI 00197998192715 listed 15 Feb 2026 Listed
Timeline
- Listed FDA GUDID 00197998192715
- Registered EUDAMED 01979988401010000000050MJ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Solventum™
- Generic name
- Surgical hair clippers
- Device name
- Surgical Clipper with Pivoting Head
- Model / Ref / Catalog
- 9668L
- Primary DI / UDI-DI
- 00197998192715
- Basic UDI-DI
- 01979988401010000000050MJ
- FDA product code
- LWK
- EMDN code
- V9099 Various devices not included in other classes - other
- GMDN term
- Surgical hair clippers
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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