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WEPA Nasendusche

by Euro Vital Pharma GmbH

Ref 60016922

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 Number42519286P00018301B29 Basic UDI-DI 04251928600797UDI-DIDate14 Sep 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  • Withdrawn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
WEPA Nasendusche (mit Nasenspülsalz)
Model / Reference
60016922
Primary DI / UDI-DI
04251928600797
Basic UDI-DI
42519286P00018301B29
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class IIa
Medical Purpose
Nasenspülsalz is a medical device intended to be used for nasal irrigation. Nasenspülsalz is a 100% sodium chloride (NaCl) intended to be dissolved in water in physiological (isotonic, 0.9%) or hypertonic concentration (2.6%).

Manufacturer details

EUDAMED SRN
DE-PR-000053356

Other devices from Euro Vital Pharma GmbH

See all devices from Euro Vital Pharma GmbH →

Properties

Other properties (1)

  • Sterile: No