TraumaFix
by Reliance Medical Ltd 2 variants
Ref X9551
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number506013188TF713Z 05060497996533 | Date5 Feb 2025 | StatusActive |
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- Withdrawn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
- Cardboard Splint
- Model / Reference
- X9551
- Primary DI / UDI-DI
- 05060497996533
- Basic UDI-DI
- 506013188TF713Z
- Direct Marketing DI
- 05060497996533
- EMDN Code
- M030599 Immobilisation systems and devices - other
- Device Class
- Class I
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- GB-MF-000004799
- Authorised representative
- Reliance Medical (Ireland) IE-AR-000003675
Other devices from Reliance Medical Ltd
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: 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