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FONA procedure pack 13G, adult - innovative ventilation

by innovative ventilation Vertriebsgesellschaft mbH

Ref IV2618301

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4270004381207QA Basic UDI-DI 04270004381207UDI-DIDate16 May 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
FONA procedure pack 13G, adult - innovative ventilation
Model / Reference
IV2618301
Primary DI / UDI-DI
04270004381207
Basic UDI-DI
4270004381207QA
EMDN Code
Z1203019085 Various instruments for anaesthesia and pulmonary ventilation support - consumables
Device Class
Class IIa
Medical Purpose
Combination of Cricotomy canula and ventilation device to perform oxygenation through a front-of-neck-access in emergency cases.

Manufacturer details

EUDAMED SRN
DE-PR-000041965

Other devices from innovative ventilation Vertriebsgesellschaft mbH

Properties

  • Sterile