SenSura
Ref 15030
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 | Number57089322975108G | 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- Withdrawn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 ostomy bag 1-piece closed
- Model / Reference
- 15030
- Primary DI / UDI-DI
- 05708932749435, 05708932727709, 05708932479998, 05708932454988, 05701780179478, 05701780274128, 05708932743631, 05708932752527, 05708932454520, 05708932481052
- Basic UDI-DI
- 57089322975108G
- Unit of Use DI
- 05708932749411, 05701780126144, 05701780126090, 05701780126106, 05708932786829, 05701780274012, 05708932786836, 05708932752534, 05701780126120, 05701780126137
- EMDN Code
- A1001010102, A1001020102
- Device Class
- Class I
- EU market of registration
- PortugalEstoniaSlovakiaItalyLithuaniaSpainHungaryCyprusBelgiumCzechia
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