<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>09120064420031</udiDi>
    <basicUdiDi>912006442010-00080NN</basicUdiDi>
    <tradeName>AngE Pro 8</tradeName>
    <deviceName>AngioExperience PRO8</deviceName>
    <manufacturerName>Sonotechnik Austria Angio Experience GmbH</manufacturerName>
    <manufacturerSrn>AT-MF-000000281</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0199</emdnCode>
    <emdnDescription>ARTERIO-VENOUS DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>010-00080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:36:52.466Z</lastUpdated>
  </row>
  <row>
    <udiDi>09120064420024</udiDi>
    <basicUdiDi>912006442010-00040NA</basicUdiDi>
    <tradeName>AngE Pro 4</tradeName>
    <deviceName>AngioExperience PRO4</deviceName>
    <manufacturerName>Sonotechnik Austria Angio Experience GmbH</manufacturerName>
    <manufacturerSrn>AT-MF-000000281</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0199</emdnCode>
    <emdnDescription>ARTERIO-VENOUS DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>010-00040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:36:51.659Z</lastUpdated>
  </row>
  <row>
    <udiDi>09120064420017</udiDi>
    <basicUdiDi>912006442010-00020N4</basicUdiDi>
    <tradeName>AngE Phlebo</tradeName>
    <deviceName>AngioExperience PHLEBO</deviceName>
    <manufacturerName>Sonotechnik Austria Angio Experience GmbH</manufacturerName>
    <manufacturerSrn>AT-MF-000000281</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0199</emdnCode>
    <emdnDescription>ARTERIO-VENOUS DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>010-00020</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:36:50.968Z</lastUpdated>
  </row>
</eudamedExport>