Felfúró vezető
by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft. 2 variants
Part of a family of 60 devices: see the family page
Ref 210900003
Felfúró vezető (210900003) is a Class I device made by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft., registered in EUDAMED on 5 Jan 2024 (Basic UDI-DI 5996527658GUIDDVNSTQA), active as of 22 Oct 2026.
Active
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 | Number5996527658GUIDDVNSTQA 05996527003837 | Date5 Jan 2024 | StatusActive |
Official records
- EUDAMED public site 5996527658GUIDDVNSTQA
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- Withdrawn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
- Guiding Devices
- Model / reference
- 210900003
- Primary DI / UDI-DI
- 05996527003837
- Basic UDI-DI
- 5996527658GUIDDVNSTQA
- EMDN code
- L0999 Orthopaedic and traumatological surgery instruments, reusable - other
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- HU-MF-000006772
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