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89526002

by Richard Wolf GmbH

Ref 8952.6002Model 10000201545

89526002 (8952.6002) is a device classified as Class I in the EU and Class II in the US made by Richard Wolf GmbH, registered in EUDAMED on 14 Oct 2026 (Basic UDI-DI B-04055207058169) and listed in FDA GUDID since 21 Jul 2017 (UDI-DI 04055207058169), 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-04055207058169 Basic UDI-DI 04055207058169UDI-DIDate14 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207058169 UDI-DI Date21 Jul 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207058169 registered 14 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207058169 listed 21 Jul 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207058169
  2. Registered EUDAMED B-04055207058169

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  • Withdrawn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 biopsy forceps, reusable
Device name
Modular grasping forceps, non HF
Model / Ref / Catalog
10000201545, 8952.6002, 89526002
Primary DI / UDI-DI
04055207058169
Basic UDI-DI
B-04055207058169
FDA product code
OCZ
EMDN code
L060403 Endoscopic urology forceps, reusable
GMDN term
Rigid endoscopic biopsy forceps, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
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 · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201545
8952.6002
GUDID
89526002
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Rigid endoscopic biopsy forceps, reusable

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY FORCEPS, REUSABLE.

Other devices from Richard Wolf GmbH

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Properties

  • Sterilise before use
  • Reusable
  • Manufacturing date
Other properties (22, all answered No)