<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>00733132607792</udiDi>
    <basicUdiDi>B-00733132607792</basicUdiDi>
    <tradeName>GORE® VIABAHN® Endoprosthesis</tradeName>
    <deviceName>GORE® VIABAHN® Endoprosthesis</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704020203</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DRUG ELUTING STENTS (DES)</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>PAC050502</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:09:20.918Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132607785</udiDi>
    <basicUdiDi>B-00733132607785</basicUdiDi>
    <tradeName>GORE® VIABAHN® Endoprosthesis</tradeName>
    <deviceName>GORE® VIABAHN® Endoprosthesis</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P0704020203</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR DRUG ELUTING STENTS (DES)</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>PAC050202</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:09:18.505Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132600946</udiDi>
    <basicUdiDi>B-00733132600946</basicUdiDi>
    <tradeName>GORE® ACUSEAL Cardiovascular Patch</tradeName>
    <deviceName>GORE® ACUSEAL Cardiovascular Patch</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P07020202</emdnCode>
    <emdnDescription>PTFE VASCULAR PATCHES</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>1CVX103</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:08:12.007Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132600939</udiDi>
    <basicUdiDi>B-00733132600939</basicUdiDi>
    <tradeName>GORE® ACUSEAL Cardiovascular Patch</tradeName>
    <deviceName>GORE® ACUSEAL Cardiovascular Patch</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P07020202</emdnCode>
    <emdnDescription>PTFE VASCULAR PATCHES</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>1CVX102</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:08:11.211Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132600922</udiDi>
    <basicUdiDi>B-00733132600922</basicUdiDi>
    <tradeName>GORE® ACUSEAL Cardiovascular Patch</tradeName>
    <deviceName>GORE® ACUSEAL Cardiovascular Patch</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P07020202</emdnCode>
    <emdnDescription>PTFE VASCULAR PATCHES</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>1CVX101</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:08:10.398Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132600915</udiDi>
    <basicUdiDi>B-00733132600915</basicUdiDi>
    <tradeName>GORE® ACUSEAL Cardiovascular Patch</tradeName>
    <deviceName>GORE® ACUSEAL Cardiovascular Patch</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P07020202</emdnCode>
    <emdnDescription>PTFE VASCULAR PATCHES</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>1CVX004</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:08:09.599Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132600908</udiDi>
    <basicUdiDi>B-00733132600908</basicUdiDi>
    <tradeName>GORE® ACUSEAL Cardiovascular Patch</tradeName>
    <deviceName>GORE® ACUSEAL Cardiovascular Patch</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P07020202</emdnCode>
    <emdnDescription>PTFE VASCULAR PATCHES</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>1CVX003</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:08:05.585Z</lastUpdated>
  </row>
  <row>
    <udiDi>00733132600892</udiDi>
    <basicUdiDi>B-00733132600892</basicUdiDi>
    <tradeName>GORE® ACUSEAL Cardiovascular Patch</tradeName>
    <deviceName>GORE® ACUSEAL Cardiovascular Patch</deviceName>
    <manufacturerName>W. L. Gore &amp; Associates, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000001141</manufacturerSrn>
    <authorisedRepresentativeName>W.L. Gore &amp; Associates B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000168</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P07020202</emdnCode>
    <emdnDescription>PTFE VASCULAR PATCHES</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>1CVX002</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-08-01T07:08:04.790Z</lastUpdated>
  </row>
  <row>
    <udiDi>09555952300025</udiDi>
    <basicUdiDi>955595230PVGV9</basicUdiDi>
    <tradeName>AVATAR® ePTFE Vascular Graft</tradeName>
    <deviceName>AVATAR® ePTFE Vascular Graft</deviceName>
    <manufacturerName>Biovic Sdn Bhd</manufacturerName>
    <manufacturerSrn>MY-MF-000013727</manufacturerSrn>
    <authorisedRepresentativeName>Advena Limited</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>MT-AR-000000234</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P070102020101</emdnCode>
    <emdnDescription>PTFE VASCULAR PROSTHESES, STRAIGHT, SIMPLE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>PVGRG0445</reference>
    <placedOnMarketCountry>Czechia</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:53:21.985Z</lastUpdated>
  </row>
  <row>
    <udiDi>08888893018645</udiDi>
    <basicUdiDi>8888893BMX6HV</basicUdiDi>
    <tradeName>BioMatrix Alpha Drug Eluting Coronary Stent System</tradeName>
    <deviceName>BioMatrix Alpha Drug Eluting Coronary Stent System</deviceName>
    <manufacturerName>Biosensors Europe SA</manufacturerName>
    <manufacturerSrn>CH-MF-000015764</manufacturerSrn>
    <authorisedRepresentativeName>NVT GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000006441</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P070402010301</emdnCode>
    <emdnDescription>CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BMX6-2209</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:12:03.266Z</lastUpdated>
  </row>
  <row>
    <udiDi>06931473304439</udiDi>
    <basicUdiDi>69314733LP01QL</basicUdiDi>
    <tradeName>LaaGuarder</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Shanghai Shenqi Medical Technology Co., Ltd.</manufacturerName>
    <manufacturerSrn>CN-MF-000013667</manufacturerSrn>
    <authorisedRepresentativeName>CMC Medical Devices &amp; Drugs SL</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>ES-AR-000000293</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P07040399</emdnCode>
    <emdnDescription>HEART AND CORONARY DEFECT OCCLUDERS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LP0121</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-31T15:49:45.134Z</lastUpdated>
  </row>
  <row>
    <udiDi>05413206220977</udiDi>
    <basicUdiDi>5413206UMTCS</basicUdiDi>
    <tradeName>Ultimaster Tansei</tradeName>
    <deviceName>Ultimaster Tansei Sirolimus eluting coronary stent system</deviceName>
    <manufacturerName>TERUMO EUROPE N.V.</manufacturerName>
    <manufacturerSrn>BE-MF-000001434</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P070402010301</emdnCode>
    <emdnDescription>CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DE-RQ2515KSM</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-31T08:00:19.416Z</lastUpdated>
  </row>
  <row>
    <udiDi>05413206220953</udiDi>
    <basicUdiDi>5413206UMTCS</basicUdiDi>
    <tradeName>Ultimaster Tansei</tradeName>
    <deviceName>Ultimaster Tansei Sirolimus eluting coronary stent system</deviceName>
    <manufacturerName>TERUMO EUROPE N.V.</manufacturerName>
    <manufacturerSrn>BE-MF-000001434</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P070402010301</emdnCode>
    <emdnDescription>CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DE-RQ2512KSM</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-31T07:52:21.573Z</lastUpdated>
  </row>
  <row>
    <udiDi>05065021834107</udiDi>
    <basicUdiDi>5065021834SYNPP010Z2</basicUdiDi>
    <tradeName>Vascular Surgery</tradeName>
    <deviceName>VAS (Vascular Surgery)</deviceName>
    <manufacturerName>SYNDEO Medical</manufacturerName>
    <manufacturerSrn>BE-PR-000044136</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P0704020299</emdnCode>
    <emdnDescription>PERIPHERAL VASCULAR STENTS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SYN-VAS02-001</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-31T06:17:18.311Z</lastUpdated>
  </row>
  <row>
    <udiDi>04260508661066</udiDi>
    <basicUdiDi>426050866DSLAOXXG2REXXXSJ</basicUdiDi>
    <tradeName>IMPERIA-M Delivery System</tradeName>
    <deviceName>IMPERIA Delivery System</deviceName>
    <manufacturerName>NVT GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000005426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P07038002</emdnCode>
    <emdnDescription>CARDIAC VALVE TRANSCATHETER IMPLANT ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DSL-AO18G2115M</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-30T23:04:27.518Z</lastUpdated>
  </row>
  <row>
    <udiDi>04260508661011</udiDi>
    <basicUdiDi>426050866THVAOXXXXG1REAC</basicUdiDi>
    <tradeName>ALLEGRA Transcatheter Heart Valve</tradeName>
    <deviceName>ALLEGRA Transcatheter Heart Valve (THV)</deviceName>
    <manufacturerName>NVT GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000005426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P070301030201</emdnCode>
    <emdnDescription>STENTED BIOLOGICAL AORTIC VALVES FOR PERCUTANEOUS IMPLANT - NON-VALVE TISSUE OF ANIMAL ORIGIN</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>THV-AO0023G1RE</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-30T23:04:25.078Z</lastUpdated>
  </row>
  <row>
    <udiDi>04260508661004</udiDi>
    <basicUdiDi>426050866DSLAOXXG1REXXXS5</basicUdiDi>
    <tradeName>ALLEGRA Delivery System TF</tradeName>
    <deviceName>ALLEGRA Delivery System transfemoral (TF)</deviceName>
    <manufacturerName>NVT GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000005426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P07038002</emdnCode>
    <emdnDescription>CARDIAC VALVE TRANSCATHETER IMPLANT ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DSL-AO18G1RE1150</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-30T23:04:22.691Z</lastUpdated>
  </row>
  <row>
    <udiDi>04260182525395</udiDi>
    <basicUdiDi>426018252MVSDPPD5</basicUdiDi>
    <tradeName>Occlutech mVSD Occluder Procedure Pack</tradeName>
    <deviceName>Occlutech mVSD Occluder Procedure Pack</deviceName>
    <manufacturerName>Occlutech GmbH</manufacturerName>
    <manufacturerSrn>DE-PR-000049872</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P07040301</emdnCode>
    <emdnDescription>CARDIAC OCCLUDERS, VENTRICULAR SEPTAL DEFECTS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>71VSD04P</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-30T22:41:21.192Z</lastUpdated>
  </row>
  <row>
    <udiDi>04260182525371</udiDi>
    <basicUdiDi>426018252MVSDFLEXII9X</basicUdiDi>
    <tradeName>Occlutech mVSD Occluder Procedure Pack</tradeName>
    <deviceName>Occlutech mVSD Occluder Procedure Pack</deviceName>
    <manufacturerName>Occlutech GmbH</manufacturerName>
    <manufacturerSrn>DE-PR-000049872</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P07040301</emdnCode>
    <emdnDescription>CARDIAC OCCLUDERS, VENTRICULAR SEPTAL DEFECTS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>71VSD04F</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-30T22:41:20.392Z</lastUpdated>
  </row>
  <row>
    <udiDi>04260182524619</udiDi>
    <basicUdiDi>426018252AFRPP2X</basicUdiDi>
    <tradeName>Occlutech Atrial Flow Regulator Procedure Pack</tradeName>
    <deviceName>Occlutech Atrial Flow Regulator Procedure Pack</deviceName>
    <manufacturerName>Occlutech GmbH</manufacturerName>
    <manufacturerSrn>DE-PR-000049872</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>P0799</emdnCode>
    <emdnDescription>VASCULAR AND CARDIAC PROSTHESES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>65AFR08LP</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-30T22:41:01.947Z</lastUpdated>
  </row>
</eudamedExport>