MPDeku Foam gerollt 200x90x14 PU210beige
Ref 3000382259
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 | Number9006399DekuFoamJ5 09006399000707 | Date18 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- Withdrawn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
- MP Deku Foam
- Model / Reference
- 3000382259
- Primary DI / UDI-DI
- 09006399000707
- Basic UDI-DI
- 9006399DekuFoamJ5
- EMDN Code
- V080702 Non active anti-decubitus medical mattresses
- Device Class
- Class I
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- AT-MF-000003497
Other devices from NEVEON Austria GmbH
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