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Αμβε Στρωμα Flex, Foam

by Ambe Ιδιωτικη Κεφαλαιουχικη Εταιρεια EL EUDAMED

Ref AMBE MATTRESS FLEX EMDN V080702

Regulatory status

as of 25 Oct 2026

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

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
"Air Foam Νοσοκομειακης Χρησης Στρωμα Ενιαιο"
Model / Reference
AMBE MATTRESS FLEX
Primary DI / UDI-DI
05214002341961
Basic UDI-DI
5214002341MATTRESSFR
EMDN Code
V080702 Non active anti-decubitus medical mattresses
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000055349

Other devices from Ambe Ιδιωτικη Κεφαλαιουχικη Εταιρεια

See all devices from Ambe Ιδιωτικη Κεφαλαιουχικη Εταιρεια →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 05214002341961|5214002341MATTRESSFR 61 fields · synced 24 Oct 2026