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Ventoux

by Flight Medical Innovations Ltd. 32 variants

Ref VX64-0001

Ventoux (VX64-0001) is a Class IIa device made by Flight Medical Innovations Ltd., registered in EUDAMED on 4 Oct 2026 (Basic UDI-DI B-07290017856483), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07290017856483 Basic UDI-DI 07290017856483UDI-DIDate4 Oct 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  • Withdrawn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
VX64-0001
Primary DI / UDI-DI
07290017856483
Basic UDI-DI
B-07290017856483
EMDN code
Z1203010585 Pulmonary ventilators for hospital use - consumables
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Romania

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)