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Hustensirup

by Euro Vital Pharma GmbH

Ref 60016809Model P000163

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 Number42519286P000163BTR Basic UDI-DI 04251928600025UDI-DIDate12 Aug 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
Hustenhonig
Model / Reference
P000163, 60016809
Primary DI / UDI-DI
04251928600025
Basic UDI-DI
42519286P000163BTR
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
Medical Purpose
Hustenhonig is intended to be used to relieve dry or irritable cough and hoarseness, to soothe the mucous membrane in case of dry or irritable cough and to support in case of sore throat. The ingredients responsible for achieving the principal intended purpose of Hustenhonig, i.e. Cetraria islandica (Iceland moss) aqueous extract and honey, act like a naturally derived demulcent, emollient and soothing balm that forms a protective layer on the irritated or inflamed mucous membrane.

Manufacturer details

EUDAMED SRN
DE-PR-000053356

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Properties

Other properties (1)

  • Sterile: No