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828051

by Richard Wolf GmbH

Ref 828.051Model 10000201521

828051 (828.051) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207009574) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207009574), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207009574 Basic UDI-DI 04055207009574UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207009574 UDI-DI Date9 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207009574 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207009574 listed 9 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207009574
  2. Registered EUDAMED B-04055207009574

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  • Withdrawn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 tissue manipulation forceps, reusable
Device name
Flexible grasping and biopsy forceps
Model / Ref / Catalog
10000201521, 828.051, 828051
Description
FLEX. GRASP. FORCEPS 5FR WL 550MM double action, TL 720 mm, non-dismantling, reusable
Primary DI / UDI-DI
04055207009574
Basic UDI-DI
B-04055207009574
FDA product code
FCL, GEN
EMDN code
L060403 Endoscopic urology forceps, reusable
GMDN term
Flexible endoscopic tissue manipulation forceps, reusable
Device class
Class I
Regulation number
876.1075, 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
Size
Length — 550 Millimeter
Outer Diameter — 1.66666666666 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201521
828.051
GUDID
828051

Related devices

Category: Flexible endoscopic tissue manipulation 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)