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Aerogen USB Controller

by Aerogen Ltd Ireland EUDAMED

Ref AG-UC1000-RB

EMDN R060101

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number539151793AG00003WE Basic UDI-DIDate12 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Model / Reference
AG-UC1000-RB
Primary DI / UDI-DI
05391517937947
Basic UDI-DI
539151793AG00003WE
Direct Marketing DI
05391517936872
EMDN Code
R060101 Cold nebulisation systems
Device Class
Class I
Market of Registration
Estonia

Manufacturer details

EUDAMED SRN
IE-MF-000004597

Other devices from Aerogen Ltd

See all devices from Aerogen Ltd →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 9ea0ab61-f45d-4aef-a796-0531690c38d3 61 fields · synced 25 Oct 2026