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Injeq IQ-Tip® Analyzer

by Injeq Oyj Finland EUDAMED

Ref Injeq 301

EMDN Z12099001

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number643006754IQA30128 Basic UDI-DIDate22 Nov 2021RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Withdrawn
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
IQ-Tip® Analyzer
Model / Reference
Injeq 301
Primary DI / UDI-DI
06430067540012
Basic UDI-DI
643006754IQA30128
Direct Marketing DI
06430067540012
EMDN Code
Z12099001 Body impedance analysers
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
FI-MF-000002930

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED ac94032d-e56e-4ea9-a3d0-538bc0ef101b 61 fields · synced 24 Oct 2026