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Aria Flex

by Medstrom LTD 5 variants

Ref 05060467211123Model No Tube

Aria Flex (05060467211123) is a Class I device made by Medstrom LTD, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 5060467215060467211123QZ), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060467215060467211123QZ Basic UDI-DI 05060467211123UDI-DIDate8 Oct 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Aria Flex
Model / reference
No Tube, 05060467211123
Primary DI / UDI-DI
05060467211123
Basic UDI-DI
5060467215060467211123QZ
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
Freyr Regulatory GmbH DE-AR-000047121

Similar devices in this category

Other devices filed under ANTI-DECUBITUS MEDICAL MATTRESSES.

Other devices from Medstrom LTD

See all devices from Medstrom LTD →

Properties

Other properties (14, all answered No)