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    <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>
  <row>
    <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>
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