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8650684

by Richard Wolf GmbH

Ref 8650.684Model 10000201058

8650684 (8650.684) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 3 Sep 2026 (Basic UDI-DI B-04055207018446) and listed in FDA GUDID since 7 Aug 2024 (UDI-DI 04055207018446), 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-04055207018446 Basic UDI-DI 04055207018446UDI-DIDate3 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207018446 UDI-DI Date7 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207018446 registered 3 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207018446 listed 7 Aug 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207018446
  2. Registered EUDAMED B-04055207018446

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  • Withdrawn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

Generic name
Rigid endoscopic tissue manipulation forceps, reusable
Device name
Opt. grasp. forceps, lower urinary tract
Model / Ref / Catalog
10000201058, 8650.684, 8650684
Description
OPT. GRASPING FORCEPS STRAIGHT double-action, for grasping foreign bodies, for sheaths from 19.5Fr, for telescope 0° Ø 4mm, with twist lock, reusable
Primary DI / UDI-DI
04055207018446
Basic UDI-DI
B-04055207018446
FDA product code
GEN
EMDN code
L060403 Endoscopic urology forceps, reusable
GMDN term
Rigid endoscopic tissue manipulation forceps, reusable
Device class
Class I
Regulation number
878.4800
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201058
8650.684
GUDID
8650684

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY FORCEPS, REUSABLE.

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Properties

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