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Goldway UT3000A/UT4000A

by Isd Meditech Sdn. Bhd. EUDAMED

Withdrawn Not intended for the EU market

Ref APP-GW110100-150RSModel ALPHA-PLUS

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number955101981MCRPAPH3 Basic UDI-DIDate25 May 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Medical chart Recording Paper
Model / Reference
ALPHA-PLUS, APP-GW110100-150RS
Primary DI / UDI-DI
09551019819622
Basic UDI-DI
955101981MCRPAPH3
Direct Marketing DI
09551019819622
EMDN Code
Z12059009 ECG data management systems
Device Class
Class I

Manufacturer details

EUDAMED SRN
MY-MF-000043531
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Isd Meditech Sdn. Bhd.

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Properties

  • Measuring Function

Other properties (12)

  • 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
  • Incorporates Medicinal Product: No