Aria Flex
Ref 05060467210683Model MH 107 cm
Aria Flex (05060467210683) is a Class I device made by Medstrom LTD, registered in EUDAMED on 6 Aug 2026 (Basic UDI-DI 5060467215060467210683S5), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number5060467215060467210683S5 05060467210683 | Date6 Aug 2026 | StatusActive |
Official records
- EUDAMED public site 5060467215060467210683S5
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- Withdrawn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
- Aria Flex
- Model / reference
- MH 107 cm, 05060467210683
- Primary DI / UDI-DI
- 05060467210683
- Basic UDI-DI
- 5060467215060467210683S5
- EMDN code
- V080702 Non active anti-decubitus medical mattresses
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- UK-MF-000045032
- Authorised representative
- Being s.r.l.s IT-AR-000010173
Similar devices in this category
Other devices filed under NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES.