Brava
Ref 12050
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 | Number57089322976729B | 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- Withdrawn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
- Brava Paste accessory to fill in skin cavities and folds
- Model / Reference
- 12050
- Primary DI / UDI-DI
- 05708932529631, 05708932519571, 05708932778657, 05708932532556, 05708932528832, 05708932528764, 05708932530217, 05701780463164, 05708932724418, 05708932605243, 05708932533928, 05708932706285, 05708932603959, 05708932645133, 05708932520362, 05708932531610, 05708932730112
- Basic UDI-DI
- 57089322976729B
- EMDN Code
- A108002 Protective creams / gels for peristomal skin
- Device Class
- Class I
- EU market of registration
- LiechtensteinItalyTürkiyeBelgiumDenmarkNorwayGermanyCyprusLithuaniaCroatiaFinlandRomaniaSloveniaCzechiaAustriaIrelandNetherlands
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