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Portkanülen-Wechsel KIT"

by Diaprax GmbH Spezialversand für Diabetikerbedarf

Ref Fresenius Kabi

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42518942B005060NJ Basic UDI-DI 04251894204548UDI-DIDate24 Sep 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  • Withdrawn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

EU market availability

Not listed: EUDAMED names no country where this device is made available.

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

Last checked 1 Nov 2026.

Specification

EUDAMED

Device Name
Portkanülen-Wechsel KIT
Model / Reference
Fresenius Kabi
Primary DI / UDI-DI
04251894204548
Basic UDI-DI
42518942B005060NJ
EMDN Code
T0203 Dressing and assistance kits
Device Class
Class III
Medical Purpose
Zum sterilen Wechsel von Portkanülen

Manufacturer details

EUDAMED SRN
DE-PR-000028677

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Properties

Other properties (1)

  • Sterile: No