Skip to content

Bronchostop Direct Adult

by HÄLSA Pharma GmbH 2 variants

Ref 9531888Model MD Marshmallow

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 Number42517781MD323PP8T Basic UDI-DI 04251778111467UDI-DIDate28 Aug 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  • Withdrawn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
MD Marshmallow, 9531888
Primary DI / UDI-DI
04251778111467
Basic UDI-DI
42517781MD323PP8T
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class IIa
Medical Purpose
The MD Marshmallow is a medical device for oral application for symptomatic treatment of any cough. It relieves dry and productive cough and soothes oral and pharyngeal irritation due to demulcent and moisturising effects on the mucosa.

Manufacturer details

EUDAMED SRN
DE-PR-000043992

Other devices from HÄLSA Pharma GmbH

See all devices from HÄLSA Pharma GmbH →

Properties

Other properties (1)

  • Sterile: No