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AirView EU BOM

by ResMed Corp. 2 variants

Ref 22241

AirView EU BOM (22241) is a Class IIa device made by Resmed Corp, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 8401934EC137LF), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8401934EC137LF Basic UDI-DI 00840193400504UDI-DIDate26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
AirView
Model / reference
22241
Primary DI / UDI-DI
00840193400504
Basic UDI-DI
8401934EC137LF
EMDN code
Z1203019092 Various instruments for anaesthesia and pulmonary ventilation support - medical device software
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000011805
Authorised representative
ResMed SAS FR-AR-000007151

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT.

Other devices from Resmed Corp

See all devices from Resmed Corp →

Properties

Other properties (14, all answered No)