Vertebris 892601108
Ref 89260.1108Model 10000201230
Vertebris 892601108 (89260.1108) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207056394) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207056394), active as of 24 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-04055207056394 04055207056394 | Date1 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207056394 | Date9 Aug 2022 | StatusListed |
Official records
- EUDAMED public site B-04055207056394
- AccessGUDID record 04055207056394
Across registries
- EUDAMED Basic UDI-DI B-04055207056394 registered 1 Sep 2026 Active
- FDA GUDID UDI-DI 04055207056394 listed 9 Aug 2022 Listed
Timeline
- Listed FDA GUDID 04055207056394
- Registered EUDAMED B-04055207056394
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Vertebris
- Generic name
- Bone trephine, reusable
- Device name
- Spinal surgery trephines
- Model / Ref / Catalog
- 10000201230, 89260.1108, 892601108
- Description
- TREPHINE Ø 6.9MM WL 210MM sharp, reusable
- Primary DI / UDI-DI
- 04055207056394
- Basic UDI-DI
- B-04055207056394
- 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
- Outer Diameter — 6.9 MillimeterLength — 210 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10000201230 89260.1108 | 892601108 |
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