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Comil

by Gruppo Farmaimpresa srl 2 variants

Ref FT.K.MDR.14.4

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 linked in EUDAMED

A group certificate may exist

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 Number805574884FTKMDR14ET Basic UDI-DI 08055748844012UDI-DIDate5 Feb 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
FT.K.MDR.14.4
Primary DI / UDI-DI
08055748844012
Basic UDI-DI
805574884FTKMDR14ET
EMDN Code
G0401 Orally administered devices for the therapy of gastro-intestinal disorders
Device Class
Class IIb
Medical Purpose
COMIL è un sistema utile in caso di disturbi dispeptici, gonfiore gastrointestinale, aerofagia e coliche gassose causate da disbiosi intestinale e in cui è necessario associare un dispositivo medico, utile a diminuire la tensione superficiale del lume enterico, ed un probiotico, utile a ripristinare la flora intestinale.

Manufacturer details

EUDAMED SRN
IT-PR-000036632

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Properties

Other properties (1)

  • Sterile: No