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Vertebris 892606004

by Richard Wolf GmbH

Ref 892606004Model 10000201230

Vertebris 892606004 is a bone trephine (EU MDD Class I; FDA Class I; FDA product code HWK, Trephine) made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207046999) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207046999), 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-04055207046999 Basic UDI-DI 04055207046999UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207046999 UDI-DI Date9 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207046999 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207046999 listed 9 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207046999
  2. Registered EUDAMED B-04055207046999

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  • Withdrawn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
Bone trephine, reusable
Device name
Spinal surgery trephines
Model / Ref / Catalog
892606004, 10000201230
Description
TREPHINE Ø 4MM WL 100MM sharp, reusable
Primary DI / UDI-DI
04055207046999
Basic UDI-DI
B-04055207046999
FDA product code
HWK
EMDN code
Z12021199 Orthopaedic endoscopy instruments - other
GMDN term
Bone trephine, reusable
Device class
Class I
Regulation number
888.4540
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 — 100 Millimeter
Outer Diameter — 4 Millimeter

Related devices

Category: Bone trephine, reusable

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
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)