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Compressor Nebulizer

by Cofoe Medical Technology Co., Ltd. EUDAMED 2 variants

Active European Union

Ref KF-WHQ-02Model KF-WHQ-01,KF-WHQ-02,KF-WHQ-07,KF-WHQ-08,KF-WHQ-09

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69507155YSSWHQ8A Basic UDI-DIDate21 Feb 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Model / Reference
KF-WHQ-01, KF-WHQ-02, KF-WHQ-07, KF-WHQ-08, KF-WHQ-09
Primary DI / UDI-DI
06950715500996
Basic UDI-DI
69507155YSSWHQ8A
EMDN Code
Z12159002 Aerosol equipment
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CN-MF-000001077
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Cofoe Medical Technology Co., Ltd.

See all devices from Cofoe Medical Technology Co., Ltd. →

Properties

Other properties (13)

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