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AeroChamber Plus*

by Trudell Medical International FDA registration: Canada EUDAMED

Ref 101501/101501123070Model 101501 EMDN R9099

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00762860001398 Basic UDI-DIDate7 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
AeroChamber Plus* DÉMONSTRATEUR Chambre d’inhalation Adultes et Enfants à partir de 6 ans
Model / Reference
101501, 101501/101501123070
Primary DI / UDI-DI
00762860001398
Basic UDI-DI
B-00762860001398
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
CA-MF-000009860
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Trudell Medical International

See all devices from Trudell Medical International →

Properties & raw data

Show properties, registry sources and raw records
  • Administering Medicine
Other properties (10)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 00762860001398|B-00762860001398 61 fields · synced 24 Oct 2026