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isla® junior сироп за кашлица

by Euro Vital Pharma GmbH

Ref 60017232Model P000178_03

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 Number42519286P00017803B37 Basic UDI-DI 04251928600957UDI-DIDate10 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  • Withdrawn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
Isländisch Moos Hustensaft Erdbeere
Model / Reference
P000178_03, 60017232
Primary DI / UDI-DI
04251928600957
Basic UDI-DI
42519286P00017803B37
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
Medical Purpose
Soothes irritated and dry throat and pharyngeal mucosa and relieves symptoms of dry cough and hoarseness

Manufacturer details

EUDAMED SRN
DE-PR-000053356

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Properties

Other properties (1)

  • Sterile: No