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892506925

by Richard Wolf GmbH

Ref 892506925Model 10000201507

892506925 is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 14 Oct 2026 (Basic UDI-DI B-04055207058114) and listed in FDA GUDID since 21 Jul 2017 (UDI-DI 04055207058114), 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-04055207058114 Basic UDI-DI 04055207058114UDI-DIDate14 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207058114 UDI-DI Date21 Jul 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207058114 registered 14 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207058114 listed 21 Jul 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207058114
  2. Registered EUDAMED B-04055207058114

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  • Withdrawn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
Endoscopic surgical probe
Device name
Probes
Model / Ref / Catalog
892506925, 10000201507
Primary DI / UDI-DI
04055207058114
Basic UDI-DI
B-04055207058114
FDA product code
NBH
EMDN code
Z12021199 Orthopaedic endoscopy instruments - other
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
888.1100
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

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - OTHER.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Manufacturing date
Other properties (21, all answered No)