<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>03770038212009</udiDi>
    <basicUdiDi>0038212F01012025ZK</basicUdiDi>
    <tradeName>FOEDORA</tradeName>
    <deviceName>FOEDORA</deviceName>
    <manufacturerName>FOEDORA</manufacturerName>
    <manufacturerSrn>FR-MF-000039740</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>V92</emdnCode>
    <emdnDescription>MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FD001</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-15T19:10:17.262Z</lastUpdated>
  </row>
</eudamedExport>