Materasso Magnistretch 9 2.0 FFWD MX EU - STV
Ref MPO223AA00026Model Materassi Antidecubito
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 | Number8020489MDALEXMAANT00179 | Date21 Oct 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- Withdrawn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
- Model / Reference
- Materassi Antidecubito, MPO223AA00026
- Primary DI / UDI-DI
- 08020489247330, 08020489247774, 08020489247798, 08020489247859, 08020489247439, 08020489247392, 08020489247408, 08020489247576, 08020489247729, 08020489247583, 08020489247347, 08020489247880, 08020489247460, 08020489247378, 08020489247521, 08020489247743, 08020489247682, 08020489247415, 08020489247644, 08020489247668, 08020489247422, 08020489247361, 08020489247613, 08020489247354, 08020489247705, 08020489247545, 08020489247491, 08020489250590, 08020489247811, 08020489247606, 08020489247842, 08020489247552, 08020489247385, 08020489247446
- Basic UDI-DI
- 8020489MDALEXMAANT00179
- EMDN Code
- V080702 Non active anti-decubitus medical mattresses
- Device Class
- Class I
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000019975
Other devices from Alessanderx SPA
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