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Vertebris 892206038

by Richard Wolf GmbH

Ref 892206038Model 10000328144

Vertebris 892206038 is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 3 Sep 2026 (Basic UDI-DI B-04055207035191) and listed in FDA GUDID since 7 Dec 2022 (UDI-DI 04055207035191), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207035191 Basic UDI-DI 04055207035191UDI-DIDate3 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207035191 UDI-DI Date7 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207035191 registered 3 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207035191 listed 7 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207035191
  2. Registered EUDAMED B-04055207035191

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  • Withdrawn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

Trade name
Vertebris
Generic name
Endoscope sheath, reusable
Device name
Spinal surgery working sleeves
Model / Ref / Catalog
892206038, 10000328144
Description
WORKING SLEEVE ID 3X5.4MM OD 3.8x6.2mm, TL 127mm, distal end straight, graduated, reusable
Primary DI / UDI-DI
04055207035191
Basic UDI-DI
B-04055207035191
FDA product code
NBH
EMDN code
Z12021199 Orthopaedic endoscopy instruments - other
GMDN term
Endoscope sheath, reusable
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: Endoscope sheath, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - OTHER.

Other devices from Richard Wolf GmbH

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Properties

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