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Axtair Xxl

by Winncare France 21 variants

Ref VMXXL-140A2-CHModel AXTAIR

Active European Union

CE MDR

Valid until

14 Apr 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberFR26/00000124 Date14 Apr 2026IssuedStatusActive EUDAMED: not on the EU market expires 14 Apr 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • FR26/00000124 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    14 Apr 2026
    Expires
    14 Apr 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Axtair
Model / Reference
AXTAIR, VMXXL-140A2-CH
Primary DI / UDI-DI
03664897036800
Basic UDI-DI
366489700083H9
Direct Marketing DI
03664897036800
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

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