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829601

by Richard Wolf GmbH

Ref 829.601Model 10000201521

829601 (829.601) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04055207009710) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04055207009710), 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-04055207009710 Basic UDI-DI 04055207009710UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207009710 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207009710 registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207009710 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207009710
  2. Registered EUDAMED B-04055207009710

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  • Withdrawn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
Flexible endoscopic biopsy forceps, reusable
Device name
Flexible grasping and biopsy forceps
Model / Ref / Catalog
10000201521, 829.601, 829601
Description
FLEX. BIOPSY FORCEPS Ø 3FR WL 920MM reusable
Primary DI / UDI-DI
04055207009710
Basic UDI-DI
B-04055207009710
FDA product code
FCL
EMDN code
L060403 Endoscopic urology forceps, reusable
GMDN term
Flexible endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
876.1075
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
Size
Outer Diameter — 1 Millimeter
Length — 920 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201521
829.601
GUDID
829601

Related devices

Category: Flexible endoscopic biopsy forceps, reusable

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY FORCEPS, REUSABLE.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

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