6126120000
Part of a family of 14 devices: see the family page
Ref 6126-120-000Model 08858251002179SW
6126120000 is a Class I device made by Stryker Corp., registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI 08858251002179SW) and listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04546540501578), 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 | Number08858251002179SW 04546540501578 | Date30 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04546540501578 | Date24 Sep 2018 | StatusListed |
Official records
- EUDAMED public site 08858251002179SW
- AccessGUDID record 04546540501578
Across registries
- EUDAMED Basic UDI-DI 08858251002179SW registered 30 Sep 2026 Active
- FDA GUDID UDI-DI 04546540501578 listed 24 Sep 2018 Listed
Timeline
- Listed FDA GUDID 04546540501578
- Registered EUDAMED 08858251002179SW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Portable/mobile rechargeable battery pack
- Device name
- Heavy Duty Charger Modules, Housings and Shields
- Model / Ref / Catalog
- 08858251002179SW EUDAMED6126-120-000 EUDAMED6126120000 GUDID
- Primary DI / UDI-DI
- 04546540501578
- Basic UDI-DI
- 08858251002179SW
- Direct marketing DI
- 04546540501578
- FDA product code
- HWE
- EMDN code
- Z12139099 Various orthopaedic and traumatology instruments - other
- GMDN term
- Portable/mobile rechargeable battery pack
- Device class
- Class I
- Regulation number
- 878.4820
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858251002179SW 6126-120-000 | 6126120000 |
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