5400700000
Ref 5400-700-000Model 08858251003756TP
5400700000 is a device classified as Class IIa in the EU and Class I in the US made by Stryker Corp., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 08858251003756TP) and listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04546540604095), active as of 7 Nov 2026.
Active
CE MDR
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/MDR EUDAMED | Number08858251003756TP 04546540604095 | Date30 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04546540604095 | Date24 Sep 2018 | StatusListed |
Official records
- EUDAMED public site 08858251003756TP
- AccessGUDID record 04546540604095
Across registries
- EUDAMED Basic UDI-DI 08858251003756TP registered 30 Oct 2026 Active
- FDA GUDID UDI-DI 04546540604095 listed 24 Sep 2018 Listed
Timeline
- Listed FDA GUDID 04546540604095
- Registered EUDAMED 08858251003756TP
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Powered bone mill motor
- Device name
- Bone Mill System
- Model / Ref / Catalog
- 08858251003756TP EUDAMED5400-700-000 EUDAMED5400700000 GUDID
- Primary DI / UDI-DI
- 04546540604095
- Basic UDI-DI
- 08858251003756TP
- Direct marketing DI
- 04546540604095
- FDA product code
- HWE
- EMDN code
- Z12019080 Various instruments for general and multidisciplinary surgery - hardware accessories
- GMDN term
- Powered bone mill motor
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 878.4820
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858251003756TP 5400-700-000 | 5400700000 |
| Device class | Class IIa | Class I |
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