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Fentex 335300FX

by FENTEX medical GmbH

Ref 335300FXModel Instrument zum Schneiden.

Fentex 335300FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04250407730376) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 04250407730376), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04250407730376 Basic UDI-DI 04250407730376UDI-DIDate7 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250407730376 UDI-DI Date12 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250407730376 registered 7 Sep 2026 Active
  • FDA GUDID UDI-DI 04250407730376 listed 12 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250407730376
  2. Registered EUDAMED B-04250407730376

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  • Withdrawn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
Nasal knife
Model / Ref / Catalog
335300FX, Instrument zum Schneiden.
Description
Rhinoplastic Knife by Joseph straight, blunt 15 cm
Primary DI / UDI-DI
04250407730376
Basic UDI-DI
B-04250407730376
FDA product code
LRC
EMDN code
L140205 Nasal and paranasal cavity surgery rasps and knives, reusable
GMDN term
Nasal knife
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: Nasal knife

Similar devices in this category

Other devices filed under NASAL AND PARANASAL CAVITY SURGERY INSTRUMENTS, REUSABLE.

Other devices from FENTEX medical GmbH

See all devices from FENTEX medical GmbH →

Properties

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