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Soin de la toux

by Aboca S.P.A. Società Agricola 2 variants

Ref 08032472031598

Active European Union

CE MDR

Valid until

2 Nov 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Eurofins Product Testing Italy S.r.l.

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/MDR Number8032472CUTOSax1G9 Basic UDI-DI 08032472031598UDI-DIDate20 Feb 2024RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.24/5371 Active

    Quality management system EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    8 Feb 2024
    Expires
    2 Nov 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Cura della tosse
Model / Reference
08032472031598
Primary DI / UDI-DI
08032472031598
Basic UDI-DI
8032472CUTOSax1G9
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
IT-MF-000029499

Other devices from Aboca S.P.A. Società Agricola

See all devices from Aboca S.P.A. Società Agricola →

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