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<eudamedExport entity="devices">
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    <udiDi>08720214004336</udiDi>
    <basicUdiDi>B-08720214004336</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-cuff1414C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:32.412Z</lastUpdated>
  </row>
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    <udiDi>08720214004329</udiDi>
    <basicUdiDi>B-08720214004329</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-cuff1414C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:26.410Z</lastUpdated>
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    <udiDi>08720214004312</udiDi>
    <basicUdiDi>B-08720214004312</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-cuff1414C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:25.204Z</lastUpdated>
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    <udiDi>08720214004305</udiDi>
    <basicUdiDi>B-08720214004305</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-cuff1414C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:24.012Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004299</udiDi>
    <basicUdiDi>B-08720214004299</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-cuff1414C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:22.816Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004282</udiDi>
    <basicUdiDi>B-08720214004282</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-cuff1214C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:16.822Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004275</udiDi>
    <basicUdiDi>B-08720214004275</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-cuff1214C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:15.610Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004268</udiDi>
    <basicUdiDi>B-08720214004268</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-cuff1214C090</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:14.402Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004251</udiDi>
    <basicUdiDi>B-08720214004251</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-cuff1214C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:13.202Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004244</udiDi>
    <basicUdiDi>B-08720214004244</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-cuff1214C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:07.196Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004237</udiDi>
    <basicUdiDi>B-08720214004237</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-cuff1214C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:05.993Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004220</udiDi>
    <basicUdiDi>B-08720214004220</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-cuff1612C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:04.797Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004213</udiDi>
    <basicUdiDi>B-08720214004213</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-cuff1612C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:01:03.600Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004206</udiDi>
    <basicUdiDi>B-08720214004206</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-cuff1612C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:56.393Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004190</udiDi>
    <basicUdiDi>B-08720214004190</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-cuff1612C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:55.198Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004183</udiDi>
    <basicUdiDi>B-08720214004183</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-cuff1612C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:53.991Z</lastUpdated>
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    <udiDi>08720214004176</udiDi>
    <basicUdiDi>B-08720214004176</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-cuff1612C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:52.814Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004169</udiDi>
    <basicUdiDi>B-08720214004169</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-cuff1412C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:46.794Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004152</udiDi>
    <basicUdiDi>B-08720214004152</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-cuff1412C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:45.590Z</lastUpdated>
  </row>
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    <udiDi>08720214004145</udiDi>
    <basicUdiDi>B-08720214004145</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-cuff1412C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:00:44.497Z</lastUpdated>
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</eudamedExport>