Skip to content

Coatron X Pro

by TECO Medical Instruments, Production + Trading GmbH Germany EUDAMED

Ref 81 101 20Model Coatron X generic product group

EMDN W0202020101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number426018278CMX81152 Basic UDI-DIDate24 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Coatron® X - Series
Model / Reference
Coatron X generic product group, 81 101 20
Primary DI / UDI-DI
04260182781067
Basic UDI-DI
426018278CMX81152
Direct Marketing DI
04260182781067
EMDN Code
W0202020101 Semi-automated coagulometers
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000022642

Other devices from TECO Medical Instruments, Production + Trading GmbH

See all devices from TECO Medical Instruments, Production + Trading GmbH →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 0a43e5f0-a3a9-4dcf-8870-a35a47a85c75 61 fields · synced 22 Oct 2026