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Dicogel Gastro

by Dicofarm Societa' per Azioni

Ref FT0117Model Sciroppo anti-reflusso ad uso pediatrico

Dicogel Gastro (FT0117) is a Class IIa device made by Dicofarm Societa' per Azioni, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-FT0117DMA), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FT0117DMA Basic UDI-DI Date26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Dicogel gastro 150 ml
Dicogel gastro 100 ml
Dicogel gastro 200 ml
Dicogel gastro 20 ml
Model / reference
Sciroppo anti-reflusso ad uso pediatrico, FT0117
Primary DI / UDI-DI
D-FT0117DMA, D-FT0117CM8, D-FT011782, D-FT0117BM6
Basic UDI-DI
B-FT0117DMA, B-FT0117CM8, B-FT011782, B-FT0117BM6
EMDN code
G0401 Orally administered devices for the therapy of gastro-intestinal disorders
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Italy
Poland

Manufacturer details

EUDAMED SRN
IT-MF-000027549

Similar devices in this category

Other devices filed under ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS.

Other devices from Dicofarm Societa' per Azioni

Properties

Other properties (12, all answered No)