<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>++EIOPA34000</udiDi>
    <basicUdiDi>++EIOPMNT2000FB</basicUdiDi>
    <tradeName>MINT Surgical Device</tradeName>
    <deviceName>MINT Device</deviceName>
    <manufacturerName>Sanoculis Ltd.</manufacturerName>
    <manufacturerSrn>IL-MF-000026403</manufacturerSrn>
    <authorisedRepresentativeName>MedNet EC-REP GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000002</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q020199</emdnCode>
    <emdnDescription>OPHTHALMIC CUTTING DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>A34-000</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-15T15:56:38.334Z</lastUpdated>
  </row>
  <row>
    <udiDi>++EIOPAS1000</udiDi>
    <basicUdiDi>++EIOPMNT2000FB</basicUdiDi>
    <tradeName>MIMS Activation Device</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Sanoculis Ltd.</manufacturerName>
    <manufacturerSrn>IL-MF-000026403</manufacturerSrn>
    <authorisedRepresentativeName>MedNet EC-REP GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000002</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q020199</emdnCode>
    <emdnDescription>OPHTHALMIC CUTTING DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>AS1000</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-15T11:46:18.109Z</lastUpdated>
  </row>
</eudamedExport>