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Invacare

by Airflo (Xiamen) Medical Co., Ltd

Ref L839Model L839 Eskal

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-06972910602589 Basic UDI-DI 06972910602589UDI-DIDate8 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
L839 Eskal
Model / Reference
L839 Eskal, L839
Primary DI / UDI-DI
06972910602589
Basic UDI-DI
B-06972910602589
EMDN Code
V080701 Active anti-decubitus medical mattresses
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000008552
Authorised representative
Share info GmbH DE-AR-000005132

Other devices from Airflo (Xiamen) Medical Co., Ltd

See all devices from Airflo (Xiamen) Medical Co., Ltd →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No