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Kijimea® Colon Irritabile Pro

by Synformulas GmbH EUDAMED

Active European Union

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberPP07498KPRO16 Basic UDI-DIDate26 Jul 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Kijimea® Reizdarm Pro
Primary DI / UDI-DI
112065742351
Unit of Use DI
111910240142
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
DE-MF-000016381

From the manufacturer

Manufacturer's product page: Kijimea K53 Advance

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