5400704000
Ref 5400-704-000Model 08858250000627S5
5400704000 is a Class I device made by Stryker Corp., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 08858250000627S5) and listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04546540604132), 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 | Number08858250000627S5 04546540604132 | Date30 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04546540604132 | Date24 Sep 2018 | StatusListed |
Official records
- EUDAMED public site 08858250000627S5
- AccessGUDID record 04546540604132
Across registries
- EUDAMED Basic UDI-DI 08858250000627S5 registered 30 Oct 2026 Active
- FDA GUDID UDI-DI 04546540604132 listed 24 Sep 2018 Listed
Timeline
- Listed FDA GUDID 04546540604132
- Registered EUDAMED 08858250000627S5
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Electrical-only medical device connection cable, reusable
- Device name
- Bone Mill Cable
- Model / Ref / Catalog
- 08858250000627S5 EUDAMED5400-704-000 EUDAMED5400704000 GUDID
- Primary DI / UDI-DI
- 04546540604132
- Basic UDI-DI
- 08858250000627S5
- Direct marketing DI
- 04546540604132
- FDA product code
- HWE
- EMDN code
- Z12019080 Various instruments for general and multidisciplinary surgery - hardware accessories
- GMDN term
- Electrical-only medical device connection cable, reusable
- Device class
- Class I
- 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 | 08858250000627S5 5400-704-000 | 5400704000 |
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