Surgimax
by Surgimax Instruments Ltd 13 variants
Ref 05-135-08Model 0426DF
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 | Number5060520350426DF7Q 05060520352497 | Date24 Aug 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- Withdrawn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
- Forceps
- Model / Reference
- 0426DF, 05-135-08
- Primary DI / UDI-DI
- 05060520352497
- Basic UDI-DI
- 5060520350426DF7Q
- Direct Marketing DI
- 05060520352497
- EMDN Code
- L03130403 Splinter forceps, reusable
- Device Class
- Class I
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- UK-MF-000042610
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Surgimax Instruments Ltd
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