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8992621

by Richard Wolf GmbH

Ref 8992.621Model 10000201431

8992621 (8992.621) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207023785) and listed in FDA GUDID since 7 Aug 2024 (UDI-DI 04055207023785), 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-04055207023785 Basic UDI-DI 04055207023785UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207023785 UDI-DI Date7 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207023785 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207023785 listed 7 Aug 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207023785
  2. Registered EUDAMED B-04055207023785

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  • Withdrawn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
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device name
Gynecological grasping forceps
Model / Ref / Catalog
10000201431, 8992.621, 8992621
Primary DI / UDI-DI
04055207023785
Basic UDI-DI
B-04055207023785
FDA product code
GEN
EMDN code
L05090399 Gynecological surgery forceps, reusable - other
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, 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
Size
Outer Diameter — 2.33333333333 Millimeter
Length — 371 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201431
8992.621
GUDID
8992621

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under OBSTETRICS AND GYNECOLOGY INSTRUMENTS, 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)