Fentex 532170FX
Ref 532170FXModel Instrument zum Halten, Fassen oder Schneiden.
Fentex 532170FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04250407742720) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 04250407742720), 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-04250407742720 04250407742720 | Date7 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250407742720 | Date12 Dec 2022 | StatusListed |
Official records
- EUDAMED public site B-04250407742720
- AccessGUDID record 04250407742720
Across registries
- EUDAMED Basic UDI-DI B-04250407742720 registered 7 Sep 2026 Active
- FDA GUDID UDI-DI 04250407742720 listed 12 Dec 2022 Listed
Timeline
- Listed FDA GUDID 04250407742720
- Registered EUDAMED B-04250407742720
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- Withdrawn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
- 532170FX, Instrument zum Halten, Fassen oder Schneiden.
- Description
- Laryngeal Grasping Forceps delicate, straight WL 23 cm
- Primary DI / UDI-DI
- 04250407742720
- Basic UDI-DI
- B-04250407742720
- FDA product code
- LRC
- EMDN code
- L140399 Larynx surgery instruments, reusable - other
- 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 LARYNX SURGERY INSTRUMENTS, REUSABLE - OTHER.