FFX ancillary
Ref 58.FXX.XXS
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number377001950357001DE | Date20 Apr 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- FFX ancillary
- Model / Reference
- 58.FXX.XXS
- Primary DI / UDI-DI
- 03770019503294, 03770019503409, 03770019503300, 03770019503584, 03770019503287, 03770019503607, 03770019503621, 03770019503423, 03770019503270, 03770019503591, 03770019503577, 03770019503614, 03770019503638, 03770019503393
- Basic UDI-DI
- 377001950357001DE
- Direct Marketing DI
- 0377001950329403770019503409037700195033000377001950358403770019503287037700195036070377001950362103770019503423037700195032700377001950359103770019503577037700195036140377001950363803770019503393
- EMDN Code
- Z12130503 Orthopaedic surgical drills
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000002722
Other devices from Sc Medica
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No