PROstep® Solo Guide
by Wright Medical Technology, Inc.
Ref 57790CADModel 08858251006866UL
PROstep® Solo Guide (57790CAD) is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 08858251006866UL), 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 | Number08858251006866UL 00889797110143 | Date27 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 08858251006866UL
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- Withdrawn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
- Prostep Mica Instrumentation - Trays and Tray Accessories- Class I -Nonsterile
- Model / reference
- 08858251006866UL, 57790CAD
- Primary DI / UDI-DI
- 00889797110143
- Basic UDI-DI
- 08858251006866UL
- Direct marketing DI
- 00889797110143
- 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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