<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>07340154900027</udiDi>
    <basicUdiDi>73401549FSEV8</basicUdiDi>
    <tradeName>Goldtrace Fetal Spiral Electrode (FSE)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Neoventa Medical AB</manufacturerName>
    <manufacturerSrn>SE-MF-000001402</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>V9099</emdnCode>
    <emdnDescription>VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CNS000004</reference>
    <placedOnMarketCountry>Sweden</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:38:49.992Z</lastUpdated>
  </row>
</eudamedExport>