T2
Ref 1830-1724SModel 08858251003290SW
T2 (1830-1724S) is a Class IIb device made by Stryker GmbH, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 08858251003290SW), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number08858251003290SW 04546540374707 | Date27 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 08858251003290SW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- T2 Humerus - Anteroposterior Intramedullary Humeral Nail - Titanium Alloy - Class Iib - Sterile
- Model / reference
- 08858251003290SW, 1830-1724S
- Primary DI / UDI-DI
- 04546540374707
- Basic UDI-DI
- 08858251003290SW
- EMDN code
- P09120201 Intramedullary nails
- Device class
- Class IIb
- EU registration type
- Standard device
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- CH-MF-000009332
- Authorised representative
- Stryker European Operations Limited IE-AR-000000092
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