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Set 200 K

by Heinz Meise GmbH

Ref 139042Model B030203.IIa.A

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 Number426048294B030203.IIa.AUK Basic UDI-DI 04260482941833UDI-DIDate3 Jul 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  • Withdrawn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

Model / Reference
B030203.IIa.A, 139042
Primary DI / UDI-DI
04260482941833
Basic UDI-DI
426048294B030203.IIa.AUK
EMDN Code
B030203 Single plasma components removal devices and kits
Device Class
Class IIa
Medical Purpose
Behandlungsset für die LDL-Apherese

Manufacturer details

EUDAMED SRN
DE-PR-000033467

Other devices from Heinz Meise GmbH

Properties

  • Sterile