899601050
Ref 899601050Model 10000201363
899601050 is a device classified as Class IIa in the EU and Class I in the US made by Richard Wolf GmbH, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-04055207071939) and listed in FDA GUDID since 12 Aug 2022 (UDI-DI 04055207047101), 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-04055207071939 | Date16 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207047101 | Date12 Aug 2022 | StatusListed |
Official records
- EUDAMED public site B-04055207071939
- AccessGUDID record 04055207047101
Across registries
- EUDAMED Basic UDI-DI B-04055207071939 registered 16 Oct 2026 Active
- FDA GUDID UDI-DI 04055207047101 listed 12 Aug 2022 Listed
Timeline
- Listed FDA GUDID 04055207047101
- Registered EUDAMED B-04055207071939
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Cannulated surgical drill bit, reusable
- Device name
- Head drills for motorized use
- Model / Ref / Catalog
- 899601050, 10000201363
- Description
- HEAD DRILL Ø 5MM cannulated Ø 2.65mm, PACK=1 PC, TIN coating, WL 145mm, reusable
- Primary DI / UDI-DI
- 04055207047101, 04055207071939
- Basic UDI-DI
- B-04055207071939, B-04055207047101
- FDA product code
- HWE
- EMDN code
- Z12130503 Orthopaedic surgical drills
- GMDN term
- Cannulated surgical drill bit, reusable
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 878.4820
- 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 — 5 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
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