5920000003
Ref 5920-000-003Model 08858251002430SF
5920000003 (5920-000-003) is a Class I device made by Stryker Corp., registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI 08858251002430SF) and listed in FDA GUDID since 22 Sep 2017 (UDI-DI 07613154598991), 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 | Number08858251002430SF 07613154598991 | Date6 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613154598991 | Date22 Sep 2017 | StatusListed |
Official records
- EUDAMED public site 08858251002430SF
- AccessGUDID record 07613154598991
Across registries
- EUDAMED Basic UDI-DI 08858251002430SF registered 6 Nov 2026 Active
- FDA GUDID UDI-DI 07613154598991 listed 22 Sep 2017 Listed
Timeline
- Listed FDA GUDID 07613154598991
- Registered EUDAMED 08858251002430SF
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical pneumatic tourniquet system
- Model / Ref / Catalog
- 08858251002430SF, 5920-000-003, 5920000003
- Primary DI / UDI-DI
- 07613154598991
- Basic UDI-DI
- 08858251002430SF
- FDA product code
- KCY
- EMDN code
- Z12139006 Pneumatic tourniquets
- GMDN term
- Surgical pneumatic tourniquet system
- Device class
- Class I
- Regulation number
- 878.5910
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 60.0 Inch
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858251002430SF 5920-000-003 | 5920000003 |
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