Skip to content

Wapiti Hoestsiroop 250 ml

by Emonta B.V.

Ref 056101, 056201

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number871175722200458 Basic UDI-DI Date16 Jan 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Trade Name
Wapiti Hoestsiroop 250 ml
Wapiti Hoestsiroop 250 ml NL/Fr
Model / Reference
056101, 056201
Primary DI / UDI-DI
08711757222004, 08711757236223
Basic UDI-DI
871175722200458, 87117572362236V
Direct Marketing DI
08711757222004
EMDN Code
Q0399 ENT devices - other
Device Class
Class I
EU market of registration
Netherlands
Belgium

Manufacturer details

EUDAMED SRN
NL-MF-000049904

Other devices from Emonta B.V.

Properties

Other properties (13)

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