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FisioEnema

by Casen Recordati, S.L. EUDAMED

Active European Union

Ref 240303.1Model FisioEnema 250 ml

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8437013001FISIOENEMAXC Basic UDI-DIDate19 May 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  • Withdrawn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

Model / Reference
FisioEnema 250 ml, 240303.1
Primary DI / UDI-DI
08437013001342
Basic UDI-DI
8437013001FISIOENEMAXC
Direct Marketing DI
08437013001342
EMDN Code
G05 Topical anorectal administered gastro-intestinal system devices
Device Class
Class IIb
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000002442

Other devices from Casen Recordati, S.L.

Properties

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