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<eudamedExport entity="devices">
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    <udiDi>08720214003933</udiDi>
    <basicUdiDi>B-08720214003933</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1210C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:51.551Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003926</udiDi>
    <basicUdiDi>B-08720214003926</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1010C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:44.351Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003919</udiDi>
    <basicUdiDi>B-08720214003919</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1010C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:43.161Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003902</udiDi>
    <basicUdiDi>B-08720214003902</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1010C040</reference>
    <placedOnMarketCountry>Bulgaria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:41.946Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003896</udiDi>
    <basicUdiDi>B-08720214003896</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3612B160</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:40.737Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003889</udiDi>
    <basicUdiDi>B-08720214003889</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3612B140</reference>
    <placedOnMarketCountry>Estonia</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:34.737Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003872</udiDi>
    <basicUdiDi>B-08720214003872</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3612B130</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:33.532Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003865</udiDi>
    <basicUdiDi>B-08720214003865</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3612B120</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:32.329Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003858</udiDi>
    <basicUdiDi>B-08720214003858</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3612B110</reference>
    <placedOnMarketCountry>Czechia</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:31.132Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003841</udiDi>
    <basicUdiDi>B-08720214003841</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3612B100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:23.929Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003834</udiDi>
    <basicUdiDi>B-08720214003834</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3412B160</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:22.747Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003827</udiDi>
    <basicUdiDi>B-08720214003827</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3412B140</reference>
    <placedOnMarketCountry>Greece</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:21.525Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003810</udiDi>
    <basicUdiDi>B-08720214003810</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3412B130</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:20.333Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003803</udiDi>
    <basicUdiDi>B-08720214003803</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3412B120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:14.332Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003797</udiDi>
    <basicUdiDi>B-08720214003797</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3412B110</reference>
    <placedOnMarketCountry>Hungary</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:13.121Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003780</udiDi>
    <basicUdiDi>B-08720214003780</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3412B100</reference>
    <placedOnMarketCountry>Finland</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:11.935Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003773</udiDi>
    <basicUdiDi>B-08720214003773</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3212B160</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:10.721Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003766</udiDi>
    <basicUdiDi>B-08720214003766</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3212B140</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:03.526Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003759</udiDi>
    <basicUdiDi>B-08720214003759</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3212B130</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:02.318Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003742</udiDi>
    <basicUdiDi>B-08720214003742</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ AAA Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704010202</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, BIFURCATED</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-AAA3212B120</reference>
    <placedOnMarketCountry>Estonia</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:01.115Z</lastUpdated>
  </row>
</eudamedExport>