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DiaSpect Tm

by EKF-diagnostic GmbH EUDAMED

Active European Union

Ref 3200-0111

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberV76 044132 0027 Date24 Jun 2026IssuedStatusActive expires 23 Jun 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Specification

EUDAMED

Device Name
Hemoglobin analyzer
Model / Reference
3200-0111
Primary DI / UDI-DI
04048534002370
Basic UDI-DI
4048534DEAAVR
Direct Marketing DI
04048534002370
EMDN Code
W0202010202 Semi-automated hematology analysers
Device Class
Class B
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006416

Other devices from Ekf Diagnostic GmbH

See all devices from Ekf Diagnostic GmbH →

Properties

  • Near-Patient Testing
  • Professional Testing
  • Surgical Instrument

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Companion Diagnostics: No
  • New Device: No