Ortholoc® 3Di
by Wright Medical Technology, Inc. 8 variants
Ref 59250075Model 08858251028171UE
Ortholoc® 3Di (59250075) is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 08858251028171UE), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number08858251028171UE 00889797022569 | Date4 Nov 2026 | StatusActive |
Official records
- EUDAMED public site 08858251028171UE
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Ortholoc 3DI Ankle Fusion Instrumentation - Trays and Tray Accessories - Class I - Nonsterile
- Model / reference
- 08858251028171UE, 59250075
- Primary DI / UDI-DI
- 00889797022569
- Basic UDI-DI
- 08858251028171UE
- Direct marketing DI
- 00889797022569
- EMDN code
- L098099 Orthopaedic and traumatological surgery instruments, reusable - other accessories
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000025260
- Authorised representative
- Stryker European Operations Limited IE-AR-000000092
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