<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>08437021705010</udiDi>
    <basicUdiDi>843702170501BX</basicUdiDi>
    <tradeName>eD-AS Anaesthesia System</tradeName>
    <deviceName>eD-AS</deviceName>
    <manufacturerName>TEMEL S.A.</manufacturerName>
    <manufacturerSrn>ES-MF-000001321</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z1203010101</emdnCode>
    <emdnDescription>ANAESTHESIA DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>eD-AS</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-03T12:11:13.780Z</lastUpdated>
  </row>
</eudamedExport>