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Aerochamber Plus Flow-Vu

by Trudell Medical International 51 variants

Ref 108501/108501119070Model 108501

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00762860000650 Basic UDI-DI 00762860000650UDI-DIDate10 Nov 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
AeroChamber Plus* Flow-Vu* Adult Mouthpiece
Model / Reference
108501, 108501/108501119070
Primary DI / UDI-DI
00762860000650
Basic UDI-DI
B-00762860000650
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

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

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Properties

  • 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