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Fentex 170700FX

by FENTEX medical GmbH

Ref 170700FXModel Instrument zum Klemmen, Halten oder Verschließen von Gefäßen

Fentex 170700FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI 42504077054KA) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 04250407758943), active as of 25 Oct 2026.

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

CE MDR

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/MDR EUDAMED Number42504077054KA Basic UDI-DI 04250407758943UDI-DIDate7 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250407758943 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42504077054KA registered 7 Sep 2026 Active
  • FDA GUDID UDI-DI 04250407758943 listed 8 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250407758943
  2. Registered EUDAMED 42504077054KA

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Fentex
Generic name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Model / Ref / Catalog
170700FX, Instrument zum Klemmen, Halten oder Verschließen von Gefäßen
Description
Vein Press by Shea 13 cm, Ø 16 mm
Primary DI / UDI-DI
04250407758943
Basic UDI-DI
42504077054KA
Direct marketing DI
04250407758943
FDA product code
LRC
EMDN code
L07080199 Vascular surgery clamps, reusable - other
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class I
Regulation number
874.4420
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical tissue compression device

Similar devices in this category

Other devices filed under CARDIOVASCULAR SURGERY INSTRUMENTS, REUSABLE.

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Properties

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