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Portable Mesh Nebulizer

by Feellife Health Inc. United States EUDAMED

Ref Air Q+Model AeroCentre

EMDN R060101

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69343253R06010121A83 Basic UDI-DIDate4 Jun 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Portable Mesh Nebulizer
Model / Reference
AeroCentre, Air Q+
Primary DI / UDI-DI
06934325303789
Basic UDI-DI
69343253R06010121A83
Direct Marketing DI
06934325303789
EMDN Code
R060101 Cold nebulisation systems
Device Class
Class IIa
Market of Registration
Germany

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 7170cca4-a44b-4cf3-8475-ba7338247203 61 fields · synced 24 Oct 2026