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Medical Mesh Nebulizer

by Feellife Health Inc. FDA registration: China EUDAMED

Ref AirICU Мах+ EMDN R060101

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69343253R06010125F8R Basic UDI-DIDate14 May 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Medical Mesh Nebulizer
Model / Reference
AirICU Мах+
Primary DI / UDI-DI
06934325306773
Basic UDI-DI
69343253R06010125F8R
Direct Marketing DI
06934325306773
EMDN Code
R060101 Cold nebulisation systems
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000000782
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Feellife Health Inc.

See all devices from Feellife Health Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 960d5b47-7e2d-4e06-938b-fdd5232fab42 61 fields · synced 24 Oct 2026