<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>00763000304423</udiDi>
    <basicUdiDi>0763000B00002016S</basicUdiDi>
    <tradeName>00763000304423</tradeName>
    <deviceName>NON-STERILE CABLES</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0280</emdnCode>
    <emdnDescription>ARRYTHMOLOGY DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>05328</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:38.213Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000301330</udiDi>
    <basicUdiDi>0763000B00000066S</basicUdiDi>
    <tradeName>Affinity™</tradeName>
    <deviceName>Affinity Emergency Handcrank</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C030180</emdnCode>
    <emdnDescription>EXTRACORPOREAL AND ASSISTED CIRCULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>HC150A</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:34.050Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000301323</udiDi>
    <basicUdiDi>0763000B00000056Q</basicUdiDi>
    <tradeName>Affinity™ CP</tradeName>
    <deviceName>Affinity CP Adapter</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C030180</emdnCode>
    <emdnDescription>EXTRACORPOREAL AND ASSISTED CIRCULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>AP40AST</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:33.242Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000268725</udiDi>
    <basicUdiDi>0763000B000006172</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>POWER CORD</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020180</emdnCode>
    <emdnDescription>CARDIAC ELECTROPHYSIOLOGY AND MAPPING DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1038SW</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:32.441Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000228699</udiDi>
    <basicUdiDi>0763000B00000266Y</basicUdiDi>
    <tradeName>00763000228699</tradeName>
    <deviceName>MANUAL RETRACTION KIT</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0280</emdnCode>
    <emdnDescription>ARRYTHMOLOGY DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>20MRK</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:31.653Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181215</udiDi>
    <basicUdiDi>0763000B00005197U</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Analyzer Adaptor Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>J01900280</emdnCode>
    <emdnDescription>IMPLANTABLE CARDIAC DEVICES PROGRAMMERS - HARDWARE ACCESSORY</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5103</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:27.651Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181208</udiDi>
    <basicUdiDi>0763000B00005187S</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Surgical Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020280</emdnCode>
    <emdnDescription>TEMPORARY CARDIAC ELECTRICAL STIMULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5832S</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:27.210Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181338</udiDi>
    <basicUdiDi>0763000B00003637M</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>ECG Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>J01900280</emdnCode>
    <emdnDescription>IMPLANTABLE CARDIAC DEVICES PROGRAMMERS - HARDWARE ACCESSORY</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>2090EC</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:26.858Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181239</udiDi>
    <basicUdiDi>0763000B00003647P</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Patient Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020280</emdnCode>
    <emdnDescription>TEMPORARY CARDIAC ELECTRICAL STIMULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5433AL</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:25.517Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181185</udiDi>
    <basicUdiDi>0763000B00008678N</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Analyzer Surgical Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>J01900280</emdnCode>
    <emdnDescription>IMPLANTABLE CARDIAC DEVICES PROGRAMMERS - HARDWARE ACCESSORY</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>2292</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:06.790Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181116</udiDi>
    <basicUdiDi>0763000B00008688Q</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Disposable Safety Patient Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020280</emdnCode>
    <emdnDescription>TEMPORARY CARDIAC ELECTRICAL STIMULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5846AL</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:05.996Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000181093</udiDi>
    <basicUdiDi>0763000B00008698S</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Disposable Surgical Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020280</emdnCode>
    <emdnDescription>TEMPORARY CARDIAC ELECTRICAL STIMULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5833SL</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:05.188Z</lastUpdated>
  </row>
  <row>
    <udiDi>00643169889675</udiDi>
    <basicUdiDi>0763000B00005177Q</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>Patient Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020280</emdnCode>
    <emdnDescription>TEMPORARY CARDIAC ELECTRICAL STIMULATION DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5492AL</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:05:04.395Z</lastUpdated>
  </row>
  <row>
    <udiDi>00643169496095</udiDi>
    <basicUdiDi>0763000B00000597F</basicUdiDi>
    <tradeName>00643169496095</tradeName>
    <deviceName>AUTO CONNECTION BOX</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020180</emdnCode>
    <emdnDescription>CARDIAC ELECTROPHYSIOLOGY AND MAPPING DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>2037A</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:04:59.597Z</lastUpdated>
  </row>
  <row>
    <udiDi>00199150062911</udiDi>
    <basicUdiDi>0763000B00026288G</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName>System Cart</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020180</emdnCode>
    <emdnDescription>CARDIAC ELECTROPHYSIOLOGY AND MAPPING DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>AFR-00213</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:04:46.516Z</lastUpdated>
  </row>
  <row>
    <udiDi>00199150027613</udiDi>
    <basicUdiDi>0763000B00026268C</basicUdiDi>
    <tradeName>Sphere-360™</tradeName>
    <deviceName>Extension Cable</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C020180</emdnCode>
    <emdnDescription>CARDIAC ELECTROPHYSIOLOGY AND MAPPING DEVICES - ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>AFR-00022-C</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:04:39.314Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000307837</udiDi>
    <basicUdiDi>B-00763000307837</basicUdiDi>
    <tradeName>TYRX™</tradeName>
    <deviceName>TYRX Absorbable Antibacterial Env Med</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>AIMDD</riskClass>
    <legislation>AIMDD</legislation>
    <emdnCode>P900201</emdnCode>
    <emdnDescription>POLYGLYCOLIC ACID AND ASSOCIATIONS MESHES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CMRM6122INT</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-04T15:32:17.383Z</lastUpdated>
  </row>
  <row>
    <udiDi>00643169740402</udiDi>
    <basicUdiDi>B-00643169740402</basicUdiDi>
    <tradeName>IN.PACT™ Admiral™</tradeName>
    <deviceName>IN.PACT Admiral</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>C010402020199</emdnCode>
    <emdnDescription>PTA DILATATION CATHETERS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SBI05012013P</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-04T14:39:07.492Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000756925</udiDi>
    <basicUdiDi>0763000B00006898N</basicUdiDi>
    <tradeName>RapidCross™</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C010402020101</emdnCode>
    <emdnDescription>PTA BALLOON DILATATION CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>A14BX035060170</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-30T19:47:12.799Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000756970</udiDi>
    <basicUdiDi>0763000B00006898N</basicUdiDi>
    <tradeName>RapidCross™</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C010402020101</emdnCode>
    <emdnDescription>PTA BALLOON DILATATION CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>A14BX035120090</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-30T19:47:12.777Z</lastUpdated>
  </row>
</eudamedExport>