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Axtair Automorpho Plus

by Winncare France France EUDAMED

Ref VKAUTOP-090G3G-ILModel AXTAIR

EMDN V080701

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberFR26/00000124 Date14 Apr 2026IssuedStatusActive expires 14 Apr 2031

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • FR26/00000124 Issued

    Quality management system EU MDR

    Notified body
    Notified body 1639
    Issued
    14 Apr 2026
    Expires
    14 Apr 2031

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Axtair
Model / Reference
AXTAIR, VKAUTOP-090G3G-IL
Primary DI / UDI-DI
03664897033878
Basic UDI-DI
366489700083H9
EMDN Code
V080701 Active anti-decubitus medical mattresses
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
FR-MF-000000482

Other devices from Winncare France

See all devices from Winncare France →

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 35027092-0508-4f9f-9360-75f748f666bf 61 fields · synced 22 Oct 2026