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gasimetin simetikon kapi 0+

by Gruppo Farmaimpresa SRL Italy EUDAMED

Ref FT.MDR.16 EMDN G99

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805574884FTCE16-267U Basic UDI-DIDate19 May 2023RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
RILEX GTT 20ml
Model / Reference
FT.MDR.16
Primary DI / UDI-DI
08606015668291
Basic UDI-DI
805574884FTCE16-267U
EMDN Code
G99 Gastrointestinal devices - other
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IT-MF-000012625

Other devices from Gruppo Farmaimpresa SRL

See all devices from Gruppo Farmaimpresa SRL →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED ada31a07-1d4c-412d-b7d5-c5bd7ae4c825 61 fields · synced 24 Oct 2026