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VORTEX with adult mask

by PARI GmbH Spezialisten für effektive Inhalation 6 variants

Ref 051G5067Model VORTEX with adult mask

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426002043-S051-5060-00R2 Basic UDI-DI 04251855901691UDI-DIDate16 Jul 2026RegisteredStatusActive

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  • Withdrawn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
VORTEX with adult mask
Model / Reference
VORTEX with adult mask, 051G5067
Primary DI / UDI-DI
04251855901691
Basic UDI-DI
426002043-S051-5060-00R2
EMDN Code
R900901 Inhalers
Device Class
Class IIa
Medical Purpose
The VORTEX is a holding chamber. It is used in conjunction with medication sprays, the so called metered dose inhalers for treatment of the lower airways. The VORTEX masks are accessories for treatment using a PARI holding chamber. They enable inhalation of aerosol through the mouth and nose.

Manufacturer details

EUDAMED SRN
DE-PR-000032641

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Properties

Other properties (1)

  • Sterile: No