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Vortex

by PARI GmbH Spezialisten für effektive Inhalation 10 variants

Ref 051G5002Model VORTEX > 4 years

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426002043-P051-5000-00KH Basic UDI-DI 04251855901561UDI-DIDate28 Nov 2025RegisteredStatusActive

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  • Withdrawn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
Model / Reference
VORTEX > 4 years, 051G5002
Primary DI / UDI-DI
04251855901561
Basic UDI-DI
426002043-P051-5000-00KH
Direct Marketing DI
04251855902230
EMDN Code
R900901 Inhalers
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
DE-MF-000006567

Other devices from PARI GmbH Spezialisten für effektive Inhalation

See all devices from PARI GmbH Spezialisten für effektive Inhalation →

Properties

  • Administering Medicine

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No