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Sistema di aspirazione Vuoto

by Behringer S.R.L.

Ref Sistema di aspirazione VuotoModel Medical gas/vacuum pipeline systems

Active European Union

CE MDR

Valid until

14 Mar 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier KIWA CERMET ITALIA S.P.A.

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 NumberMDR 00022-A Date20 Oct 2026IssuedStatusActive expires 14 Mar 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 00022-A Active

    Quality management system EU MDR

    Issued
    20 Oct 2026
    Expires
    14 Mar 2029

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Medical gas/vacuum pipeline systems, Sistema di aspirazione Vuoto
Primary DI / UDI-DI
08054154121373
Basic UDI-DI
805415412IGMG8
Direct Marketing DI
08054154121373
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class IIb
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000023450

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Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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