SenSura Mio Convex
Ref 13680
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 | Number57089322975689F | Date17 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- Withdrawn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 urostomy bag 1-piece
- Model / Reference
- 13680
- Primary DI / UDI-DI
- 05701780436557, 05701780436700, 05701780436649, 05701780250320, 05701780251105, 05701780249294, 05701780249546, 05701780436670, 05701780249263, 05701780436588, 05701780250092, 05701780436618
- Basic UDI-DI
- 57089322975689F
- Unit of Use DI
- 05701780436571, 05701780436793, 05701780436663, 05701780250306, 05701780251082, 05701780249287, 05701780249560, 05701780436694, 05701780249256, 05701780436601, 05701780250078, 05701780436632
- EMDN Code
- A1001030202 One-piece urostomy bags for retracted stoma, convex, with tissue cover
- Device Class
- Class I
- EU market of registration
- NetherlandsFinlandDenmarkIrelandNorwayGermanyLiechtenstein
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