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PARI SINUS2 Verneblersystem (DE/AT)

by PARI GmbH Spezialisten für effektive Inhalation

Ref 128G1000Model PARI SINUS2

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 Number42518559-S128-1000-00K4 Basic UDI-DI 04260020437514UDI-DIDate13 Oct 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  • Withdrawn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

Model / Reference
PARI SINUS2, 128G1000
Primary DI / UDI-DI
04260020437514
Basic UDI-DI
42518559-S128-1000-00K4
EMDN Code
R060101 Cold nebulisation systems
Device Class
Class IIa
Medical Purpose
The PARI SINUS2 nebuliser system consists of a PARI SINUS2 compressor and a PARI LC SPRINT SINUS nebuliser. The system is used for treatment of the upper airways.

Manufacturer details

EUDAMED SRN
DE-PR-000032641

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Properties

Other properties (1)

  • Sterile: No