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Grintuss lutschtabletten

by Aboca S.P.A. Società Agricola Italy EUDAMED

Ref DEGRIACOX

EMDN V9017

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-ITM29499DEGRIACOXFH Basic UDI-DIDate6 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Grintuss adulti compresse con Poliresin
Model / Reference
DEGRIACOX
Primary DI / UDI-DI
D-ITM29499DEGRIACOXFH
Basic UDI-DI
B-ITM29499DEGRIACOXFH
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000029499

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 5504f206-0e86-4f8e-bc1d-8aa6ece10027 61 fields · synced 24 Oct 2026