7900125000
Ref 7900-125-000Model 08858250000611RN
7900125000 (7900-125-000) is a Class I device made by Stryker Corp., registered in EUDAMED on 26 Jun 2026 (Basic UDI-DI 08858250000611RN) and listed in FDA GUDID since 19 Dec 2025 (UDI-DI 07613327643848), active as of 24 Oct 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 | Number08858250000611RN 07613327643848 | Date26 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327643848 | Date19 Dec 2025 | StatusListed |
Official records
- EUDAMED public site 08858250000611RN
- AccessGUDID record 07613327643848
Across registries
- EUDAMED Basic UDI-DI 08858250000611RN registered 26 Jun 2026 Active
- FDA GUDID UDI-DI 07613327643848 listed 19 Dec 2025 Listed
Timeline
- Listed FDA GUDID 07613327643848
- Registered EUDAMED 08858250000611RN
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Pin-driving power tool attachment
- Device name
- Collets
- Model / Ref / Catalog
- 08858250000611RN, 7900-125-000, 7900125000
- Primary DI / UDI-DI
- 07613327643848
- Basic UDI-DI
- 08858250000611RN
- Direct marketing DI
- 07613327643848
- FDA product code
- HWE
- EMDN code
- Z12019080 Various instruments for general and multidisciplinary surgery - hardware accessories
- GMDN term
- Pin-driving power tool attachment
- 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 | 08858250000611RN 7900-125-000 | 7900125000 |
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