<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>08437030208014</udiDi>
    <basicUdiDi>843703020801AT</basicUdiDi>
    <tradeName>CAPTURA</tradeName>
    <deviceName>CAPTURA</deviceName>
    <manufacturerName>LIGHTFIELD MEDICAL EUROPE, S.L.</manufacturerName>
    <manufacturerSrn>ES-MF-000057359</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q0299</emdnCode>
    <emdnDescription>OPHTHALMIC DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>C-26-A</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-27T01:58:49.558Z</lastUpdated>
  </row>
</eudamedExport>