<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>00763000835361</udiDi>
    <basicUdiDi>0763000B000148489</basicUdiDi>
    <tradeName>HawkOne™</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>C010402020601</emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS, DIRECTIONAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>H1-LX-INT</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:58.266Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000835378</udiDi>
    <basicUdiDi>0763000B000148489</basicUdiDi>
    <tradeName>HawkOne™</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>C010402020601</emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS, DIRECTIONAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>H1-M-INT</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:58.248Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000835385</udiDi>
    <basicUdiDi>0763000B000148489</basicUdiDi>
    <tradeName>HawkOne™</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>C010402020601</emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS, DIRECTIONAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>H1-S-INT</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:58.230Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000871796</udiDi>
    <basicUdiDi>0763000B00026268C</basicUdiDi>
    <tradeName>00763000871796</tradeName>
    <deviceName></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-00006</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:56.782Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000871963</udiDi>
    <basicUdiDi>0763000B00026288G</basicUdiDi>
    <tradeName>00763000871963</tradeName>
    <deviceName></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-00013</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:56.685Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000911089</udiDi>
    <basicUdiDi>0763000B00012327C</basicUdiDi>
    <tradeName>N/A</tradeName>
    <deviceName></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>NITRONFS</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:56.079Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941727</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900301</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.624Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941734</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900302</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.606Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941741</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900303</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.593Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941758</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900304</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.583Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941765</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900305</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.573Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941772</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900306</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.557Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941789</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900307</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.544Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941796</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900308</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.530Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941802</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900309</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.520Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941819</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900310</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.510Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000941826</udiDi>
    <basicUdiDi>0763000B00028488Y</basicUdiDi>
    <tradeName>FlexCath Cross™</tradeName>
    <deviceName></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>MDR 2017/745</legislation>
    <emdnCode>C01020101</emdnCode>
    <emdnDescription>CENTRAL I.V. SINGLE-LUMEN CATHETERS, PERIPHERAL ACCESS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>900311</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:34.501Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000954314</udiDi>
    <basicUdiDi>0763000B000262386</basicUdiDi>
    <tradeName>N/A</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>A060102</emdnCode>
    <emdnDescription>SURGICAL DRAINAGE CONNECTION MEDICAL TUBES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>AFR-00002</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:14.155Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000954338</udiDi>
    <basicUdiDi>0763000B00026268C</basicUdiDi>
    <tradeName>00763000954338</tradeName>
    <deviceName></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-00006</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:14.134Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000954352</udiDi>
    <basicUdiDi>0763000B00026278E</basicUdiDi>
    <tradeName>00763000954352</tradeName>
    <deviceName></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-00007</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-20T18:35:14.113Z</lastUpdated>
  </row>
</eudamedExport>