SenSura Flex
Ref 11303
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 | Number57089322976068W | Date17 Apr 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- Withdrawn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 Flex ostomy baseplate convex
- Model / Reference
- 11303
- Primary DI / UDI-DI
- 05708932352239, 05708932351539, 05708932384919, 05708932352352, 05701780281546, 05708932355858, 05708932134453, 05708932361453
- Basic UDI-DI
- 57089322976068W
- Unit of Use DI
- 05701780064835, 05701780064965, 05701780065092, 05701780065061, 05701780321969, 05701780065122, 05701780065153, 05708932963626
- EMDN Code
- A1002010402 Universal plates for abdominal stoma (colo-, ileo-, urostomy) with introflex stoma
- Device Class
- Class I
- EU market of registration
- NorwayIrelandNetherlandsFinlandSpainDenmarkPortugalGermany
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