Fentex 181802FX
Ref 181802FXModel Instrument zum Halten, Fassen oder Schneiden.
Fentex 181802FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04250407720360) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 04250407720360), 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-04250407720360 04250407720360 | Date7 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250407720360 | Date8 Dec 2022 | StatusListed |
Official records
- EUDAMED public site B-04250407720360
- AccessGUDID record 04250407720360
Across registries
- EUDAMED Basic UDI-DI B-04250407720360 registered 7 Sep 2026 Active
- FDA GUDID UDI-DI 04250407720360 listed 8 Dec 2022 Listed
Timeline
- Listed FDA GUDID 04250407720360
- Registered EUDAMED B-04250407720360
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Fentex
- Generic name
- Surgical soft-tissue manipulation forceps, alligator, reusable
- Model / Ref / Catalog
- 181802FX, Instrument zum Halten, Fassen oder Schneiden.
- Description
- Grasping Forceps by Heermann curved right, serrated WL 8 cm
- Primary DI / UDI-DI
- 04250407720360
- Basic UDI-DI
- B-04250407720360
- FDA product code
- LRC
- EMDN code
- L140502 Ear surgery pliers, reusable
- GMDN term
- Surgical soft-tissue manipulation forceps, alligator, reusable
- Device class
- Class I
- Regulation number
- 874.4420
- 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
Similar devices in this category
Other devices filed under EAR SURGERY PLIERS, REUSABLE.