<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>04262517240027</udiDi>
    <basicUdiDi>42625172PFORTE10Y6</basicUdiDi>
    <tradeName>Prothesoft® Forte</tradeName>
    <deviceName>Prothesoft® Forte 10</deviceName>
    <manufacturerName>DENTARA Medical UG</manufacturerName>
    <manufacturerSrn>DE-MF-000049372</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>NAT02.83</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-31T02:41:56.920Z</lastUpdated>
  </row>
</eudamedExport>