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ΑΜΒΕ MEMORY AIR FOAM ΝΟΣΟΚΟΜΕΙΑΚΗΣ ΧΡΗΣΗΣ ΣΤΡΩΜΑ 15cm, ENIAIO 120

by Ambe Ιδιωτικη Κεφαλαιουχικη Εταιρεια

Ref MEMORY 15CM 120

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5214002341MATTRESSFR Basic UDI-DI 05214002341756UDI-DIDate14 Oct 2026RegisteredStatusActive

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  • Withdrawn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
"Air Foam Νοσοκομειακης Χρησης Στρωμα Ενιαιο"
Model / Reference
MEMORY 15CM 120
Primary DI / UDI-DI
05214002341756
Basic UDI-DI
5214002341MATTRESSFR
EMDN Code
V080702 Non active anti-decubitus medical mattresses
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000055349

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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