Fentex 108715FX
Ref 108715FXModel Instrument zum Halten, Fassen oder Manipulieren.
Fentex 108715FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04250407709587) and listed in FDA GUDID since 7 Dec 2022 (UDI-DI 04250407709587), active as of 25 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-04250407709587 04250407709587 | Date7 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250407709587 | Date7 Dec 2022 | StatusListed |
Official records
- EUDAMED public site B-04250407709587
- AccessGUDID record 04250407709587
Across registries
- EUDAMED Basic UDI-DI B-04250407709587 registered 7 Sep 2026 Active
- FDA GUDID UDI-DI 04250407709587 listed 7 Dec 2022 Listed
Timeline
- Listed FDA GUDID 04250407709587
- Registered EUDAMED B-04250407709587
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Fentex
- Generic name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Model / Ref / Catalog
- 108715FX, Instrument zum Halten, Fassen oder Manipulieren.
- Description
- Dressing Forceps by Semken straight 15 cm
- Primary DI / UDI-DI
- 04250407709587
- Basic UDI-DI
- B-04250407709587
- FDA product code
- MDM
- EMDN code
- L031308 Surgical and anatomical tweezers, reusable
- GMDN term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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