<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
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    <udiDi>04262371370014</udiDi>
    <basicUdiDi>426237137000952BS</basicUdiDi>
    <tradeName>Ventilution</tradeName>
    <deviceName>Ventilution Patient Set Standard</deviceName>
    <manufacturerName>Gründler GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000025923</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>R9099</emdnCode>
    <emdnDescription>RESPIRATORY AND ANAESTHESIA DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>000070</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-01T20:27:59.771Z</lastUpdated>
  </row>
  <row>
    <udiDi>04262371370007</udiDi>
    <basicUdiDi>426237137000951BQ</basicUdiDi>
    <tradeName>Ventilution</tradeName>
    <deviceName>Ventilution Base Device</deviceName>
    <manufacturerName>Gründler GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000025923</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>R9099</emdnCode>
    <emdnDescription>RESPIRATORY AND ANAESTHESIA DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>000176</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-01T20:27:59.041Z</lastUpdated>
  </row>
</eudamedExport>