SenSura Mio Convex
Ref 16481
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 | Number57089322975969L | Date22 Jun 2026 | 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- Withdrawn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
- SenSura Mio Convex flex ostomy baseplate
- Model / Reference
- 16481
- Primary DI / UDI-DI
- 05708932895705, 05701780287258, 05701780391597, 05708932869195, 05708932895712, 05708932865722, 05708932893565, 05708932870276, 05708932595490
- Basic UDI-DI
- 57089322975969L
- Unit of Use DI
- 05708932896368, 05701780287272, 05701780391900, 05708932869201, 05708932896375, 05708932867290, 05708932894395, 05708932870283, 05708932595483
- EMDN Code
- A1002010402 Universal plates for abdominal stoma (colo-, ileo-, urostomy) with introflex stoma
- Device Class
- Class I
- EU market of registration
- DenmarkItalySloveniaIrelandGermanyNorwayNetherlandsFinlandLiechtenstein
Manufacturer details
- EUDAMED SRN
- DK-MF-000025526
Other devices from Coloplast A/S
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