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Air Comfort Deluxe V2 Bed Standard, Lustrell UK

by K Care Healthcare Solutions PTY LTD

Ref AC59217UKModel AC59XXX

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number9343062AC591115F Basic UDI-DI 09343062141030UDI-DIDate28 Aug 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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 Comfort Deluxe V2 Bed
Model / Reference
AC59XXX, AC59217UK
Primary DI / UDI-DI
09343062141030
Basic UDI-DI
9343062AC591115F
Direct Marketing DI
09343062141030
EMDN Code
Y180918 Multifunctional chairs
Device Class
Class I

Manufacturer details

EUDAMED SRN
AU-MF-000056547
Authorised representative
Advena SRL IT-AR-000051131

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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