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ASSKEA M20 avec système de récipient réutilisable

by ASSKEA GmbH EUDAMED

Active European Union

Ref 100003IST-3-MW

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426058604ProcedurePackJ4 Basic UDI-DIDate15 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Procedure Pack Device
Model / Reference
100003IST-3-MW
Primary DI / UDI-DI
04260586041767
Basic UDI-DI
426058604ProcedurePackJ4
EMDN Code
Z12159009 Equipment for removal of secretions
Device Class
Class IIa
Medical Purpose
Devices and associated accessories intended to provide suction for the removal of fluids, secretions and other substances during medical treatment.

Manufacturer details

EUDAMED SRN
DE-PR-000030721

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Properties

Other properties (1)

  • Sterile: No