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Ventoux

by Flight Medical Innovations Ltd. 32 variants

Ref Kit-0121

Ventoux (Kit-0121) is a Class IIa device made by Flight Medical Innovations Ltd., registered in EUDAMED on 1 Nov 2026 (Basic UDI-DI B-07290017856827), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-07290017856827 Basic UDI-DI 07290017856827UDI-DIDate1 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Ventoux
Model / reference
Kit-0121
Primary DI / UDI-DI
07290017856827
Basic UDI-DI
B-07290017856827
EMDN code
Z1203010599 Pulmonary ventilators for hospital use - other
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IL-MF-000025118
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under PULMONARY VENTILATORS FOR HOSPITAL USE.

Other devices from Flight Medical Innovations Ltd.

See all devices from Flight Medical Innovations Ltd. →

Properties

Other properties (12, all answered No)