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Optisana Icelandic Moss Throat Pastilles

by HCE GmbH

Ref MP-09BV3

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/MDD NumberB-MP-09BV39N Basic UDI-DI D-MP-09BV39NUDI-DIDate23 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Icelandic Moss Pastilles Mint, Isländisch Moos Halspastillen Minz-Geschmack
Model / Reference
MP-09BV3
Primary DI / UDI-DI
D-MP-09BV39N
Basic UDI-DI
B-MP-09BV39N
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class I
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
DE-MF-000028621

Other devices from HCE GmbH

See all devices from HCE GmbH →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No