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HFT750

by MEKICS Co., Ltd 2 variants

Ref MCN-WM-1875Model HFT750

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 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/MDR Number880926891Z12030104H3N Basic UDI-DI Date20 May 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
HFT750, MCN-WM-1875
Primary DI / UDI-DI
08809268914454, 08809268914317
Basic UDI-DI
880926891Z12030104H3N
EMDN Code
Z12030104 Portable pulmonary ventilators
Device Class
Class IIb
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
KR-MF-000012640
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from MEKICS Co., Ltd

  • HFT751

    Class IIb

  • MV50

    Class IIb

  • HFT750

    Class IIb

  • HFT750U

    Class II

  • MV2000

    Class IIb

  • MTV1000

    Class IIb

See all devices from MEKICS Co., Ltd →

Properties

  • Measuring Function

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
  • Administering Medicine: No
  • Incorporates Medicinal Product: No