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<eudamedExport entity="devices">
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    <udiDi>08720214004138</udiDi>
    <basicUdiDi>B-08720214004138</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-cuff1412C080</reference>
    <placedOnMarketCountry>Hungary</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:42.003Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004121</udiDi>
    <basicUdiDi>B-08720214004121</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-cuff1412C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:35.991Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004114</udiDi>
    <basicUdiDi>B-08720214004114</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-cuff1412C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:34.784Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004107</udiDi>
    <basicUdiDi>B-08720214004107</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-cuff1212C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:33.580Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004091</udiDi>
    <basicUdiDi>B-08720214004091</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-cuff1212C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:32.379Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004084</udiDi>
    <basicUdiDi>B-08720214004084</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-cuff1212C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:26.418Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004077</udiDi>
    <basicUdiDi>B-08720214004077</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-cuff1212C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:25.285Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004060</udiDi>
    <basicUdiDi>B-08720214004060</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-cuff1212C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:22.776Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004053</udiDi>
    <basicUdiDi>B-08720214004053</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-cuff1212C040</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:21.625Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004046</udiDi>
    <basicUdiDi>B-08720214004046</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-cuff1410C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:15.573Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004039</udiDi>
    <basicUdiDi>B-08720214004039</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-cuff1410C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:14.368Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004022</udiDi>
    <basicUdiDi>B-08720214004022</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-cuff1410C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:13.173Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004015</udiDi>
    <basicUdiDi>B-08720214004015</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-cuff1410C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:11.975Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004008</udiDi>
    <basicUdiDi>B-08720214004008</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-cuff1410C060</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:06.071Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003995</udiDi>
    <basicUdiDi>B-08720214003995</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-cuff1410C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:03.563Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003988</udiDi>
    <basicUdiDi>B-08720214003988</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-cuff1210C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:02.362Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003971</udiDi>
    <basicUdiDi>B-08720214003971</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-cuff1210C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:01.156Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003964</udiDi>
    <basicUdiDi>B-08720214003964</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-cuff1210C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:55.152Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003957</udiDi>
    <basicUdiDi>B-08720214003957</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-cuff1210C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:53.945Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214003940</udiDi>
    <basicUdiDi>B-08720214003940</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-cuff1210C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T00:59:52.753Z</lastUpdated>
  </row>
</eudamedExport>