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fytofontana VIROSTOP pastilles- forrest fruit flavor

by Herb-Pharma Corporation s.r.o.

Ref 10038

Active European Union

CE MDR

Valid until

18 Apr 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier 3EC International a.s.

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 Number2024-MDR/QS-023/B Date26 Jan 2026IssuedStatusActive expires 18 Apr 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2024-MDR/QS-023/B Active Supplemented

    Quality management system EU MDR

    Certifier
    3EC International a.s. 2265
    Issued
    26 Jan 2026
    Expires
    18 Apr 2029
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
fytofontana VIROSTOP pastilles
Model / Reference
10038
Primary DI / UDI-DI
18588009456107
Basic UDI-DI
85880094561003233373839ZB
EMDN Code
M9002, V9099
Device Class
Class IIa
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
SK-MF-000005839

Other devices from Herb-Pharma Corporation s.r.o.

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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