<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>04262456840005</udiDi>
    <basicUdiDi>426245684preivfMJ</basicUdiDi>
    <tradeName>04262456840005</tradeName>
    <deviceName>Univfy PreIVF Report</deviceName>
    <manufacturerName>Univfy Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000046344</manufacturerSrn>
    <authorisedRepresentativeName>Qualrep Services B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000537</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>V92</emdnCode>
    <emdnDescription>MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>UPR-001</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-01T20:34:08.880Z</lastUpdated>
  </row>
</eudamedExport>