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AeroChamber*

by Trudell Medical International FDA registration: Canada EUDAMED

Ref 82591/825114050Model 82591 EMDN R9099

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number762860MVENT1FT Basic UDI-DIDate29 Jun 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
AeroChamber* MV Holding Chamber
Model / Reference
82591, 82591/825114050
Primary DI / UDI-DI
00762860013612
Basic UDI-DI
762860MVENT1FT
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class I
Market of Registration
Spain

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 (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 00762860013612|762860MVENT1FT 61 fields · synced 23 Oct 2026