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Fentex 235101FX

by FENTEX medical GmbH

Ref 235101FXModel Instrument zum Schneiden.

Fentex 235101FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04250407723590) and listed in FDA GUDID since 9 Dec 2022 (UDI-DI 04250407723590), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04250407723590 Basic UDI-DI 04250407723590UDI-DIDate7 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250407723590 UDI-DI Date9 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250407723590 registered 7 Sep 2026 Active
  • FDA GUDID UDI-DI 04250407723590 listed 9 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250407723590
  2. Registered EUDAMED B-04250407723590

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Fentex
Generic name
Rigid endoscopic biopsy forceps, reusable
Model / Ref / Catalog
235101FX, Instrument zum Schneiden.
Description
Antrum Punch by Ostrum left backwards, with flush connector WL 10 cm, bite 2.5 mm
Primary DI / UDI-DI
04250407723590
Basic UDI-DI
B-04250407723590
FDA product code
LRC
EMDN code
L149012 ENT surgery punches, reusable
GMDN term
Rigid endoscopic biopsy forceps, 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

Related devices

Category: ENT soft-tissue cutting forceps

Similar devices in this category

Other devices filed under ENT SURGERY PUNCHES, REUSABLE.

Other devices from FENTEX medical GmbH

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)