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Aerochamber Plus Flow-Vu

by Trudell Medical International 51 variants

Ref 108504/108504119050

Active European Union

CE MDR

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/MDR Number762860VHC1NL Basic UDI-DI 00762860000643UDI-DIDate29 Jun 2022RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Valved Holding Chamber
Model / Reference
108504/108504119050
Primary DI / UDI-DI
00762860000643
Basic UDI-DI
762860VHC1NL
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class I
EU market of registration
Ireland

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

  • 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