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MVA2 VIPROXY 1touch

by Cavagna Group S.p.A. 30 variants

Ref MVA2EOS003Model VIPROXY 1touch

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-MVA2EOS003FE Basic UDI-DI D-MVA2EOS003FEUDI-DIDate12 Oct 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  • Withdrawn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
MVA2
Model / Reference
VIPROXY 1touch, MVA2EOS003
Primary DI / UDI-DI
D-MVA2EOS003FE
Basic UDI-DI
B-MVA2EOS003FE
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000028356

Other devices from Cavagna Group S.p.A.

See all devices from Cavagna Group S.p.A. →

Properties

  • Administering Medicine

Other properties (10)

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