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ASSKEA proVisioBasic

by ASSKEA GmbH 2 variants

Ref 100738-1-MW

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426058604ProcedurePackJ4 Basic UDI-DI 04260586042344UDI-DIDate15 Apr 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Procedure Pack Device
Model / Reference
100738-1-MW
Primary DI / UDI-DI
04260586042344
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

Other devices from ASSKEA GmbH

See all devices from ASSKEA GmbH →

Properties

Other properties (1)

  • Sterile: No