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Sistema Clinical Care II 220cm

by MOVI S.p.A.

Ref 98000220Model SISTEMI ANTIDECUBITO ATTIVI

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805418176AV08070188 Basic UDI-DI 08056814473976UDI-DIDate22 Jul 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
SISTEMI ANTIDECUBITO ATTIVI, 98000220
Primary DI / UDI-DI
08056814473976
Basic UDI-DI
805418176AV08070188
EMDN Code
V080701 Active anti-decubitus medical mattresses
Device Class
Class I
Medical Purpose
Il sistema è indicato per l’alleviamento delle piaghe da pressione e/o la loro prevenzione

Manufacturer details

EUDAMED SRN
IT-PR-000050873

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Properties

Other properties (1)

  • Sterile: No