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Zetalax 4000

by Fairpharm Vertriebs GmbH EUDAMED

Active European Union

Ref 04260753841695Model E0735A01

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426075384E0735A01Q5 Basic UDI-DIDate27 Jan 2026RegisteredStatusActive

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  • Withdrawn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
Macrogol 4000 powder for oral solution (with excipients) (10.7 g)
Model / Reference
E0735A01, 04260753841695
Primary DI / UDI-DI
04260753841695
Basic UDI-DI
426075384E0735A01Q5
Unit of Use DI
04260753841701
EMDN Code
G0401 Orally administered devices for the therapy of gastro-intestinal disorders
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
DE-MF-000016959

Other devices from Fairpharm Vertriebs GmbH

See all devices from Fairpharm Vertriebs GmbH →

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