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moduflex 2500

by modul technik GmbH

Ref moduflex 2500Model Medizinische Versorgungseinheit

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  • Withdrawn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
DVE starr
Model / Reference
Medizinische Versorgungseinheit, moduflex 2500
Primary DI / UDI-DI
04262419580092
Basic UDI-DI
426241958DVEst3M8
Direct Marketing DI
04262419580092
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

From the manufacturer

Manufacturer's product page: moduflex 2500

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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