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moduversa HM plus

by modul technik GmbH

Ref moduversa HM plusModel Medizinische Versorgungseinheiten

Active European Union

CE MDR

Valid until

2 Dec 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV NORD CERT GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number44911222228 Date3 Dec 2025IssuedStatusActive expires 2 Dec 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 44911222228 Active

    Quality management system EU MDR

    Certifier
    TÜV NORD CERT GmbH 0044
    Issued
    3 Dec 2025
    Expires
    2 Dec 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Typenreihe DVE beweglich
Model / Reference
Medizinische Versorgungseinheiten, moduversa HM plus
Primary DI / UDI-DI
04262419580047
Basic UDI-DI
426241958DVEbe9HJ
Direct Marketing DI
04262419580047
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000014647

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Properties

  • Administering Medicine

Other properties (12)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No