<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>04260717720066</udiDi>
    <basicUdiDi>426071772XT230008Z</basicUdiDi>
    <tradeName>XtremeCT II</tradeName>
    <deviceName></deviceName>
    <manufacturerName>SCANCO Medical AG</manufacturerName>
    <manufacturerSrn>CH-MF-000016419</manufacturerSrn>
    <authorisedRepresentativeName>Axxos GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005590</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z11039099</emdnCode>
    <emdnDescription>VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS – OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>XT23000</reference>
    <placedOnMarketCountry>Denmark</placedOnMarketCountry>
    <lastUpdated>2026-07-01T20:01:59.486Z</lastUpdated>
  </row>
</eudamedExport>