FootLocker® Lower Extremity Systems
Ref IN2002Model FootLocker™ - Class Ir Reusable Surgical Instrumentation
Withdrawn
CE MDR, withdrawn
Ended
Withdrawn
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number5051693AAA0001IYV 15051693000961 | Date18 Jun 2026 | StatusWithdrawn |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Withdrawn
Specification
- Device Name
- FootLocker™ - Class Ir Reusable Surgical Instrumentation
- Model / Reference
- FootLocker™ - Class Ir Reusable Surgical Instrumentation, IN2002
- Primary DI / UDI-DI
- 15051693000961
- Basic UDI-DI
- 5051693AAA0001IYV
- EMDN Code
- P090680 Foot prostheses - accessories
- Device Class
- Class I
Manufacturer details
- EUDAMED SRN
- UK-MF-000048004
- Authorised representative
- Arazy Group (Ireland) Ltd. IE-AR-000000093
Other devices from Implants International Ltd
Properties
Other properties (11)
- 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
- Incorporates Medicinal Product: No