<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>00850017630338</udiDi>
    <basicUdiDi>0850017630VTCE21XM</basicUdiDi>
    <tradeName>LimFlow Vector</tradeName>
    <deviceName>LimFlow Vector</deviceName>
    <manufacturerName>LimFlow SA</manufacturerName>
    <manufacturerSrn>FR-MF-000011529</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C01901901</emdnCode>
    <emdnDescription>VEIN STRIPPER DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>VT-CE-21</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T03:15:43.225Z</lastUpdated>
  </row>
  <row>
    <udiDi>00887482048504</udiDi>
    <basicUdiDi>08401132StripperHZ</basicUdiDi>
    <tradeName>Symmetry ®</tradeName>
    <deviceName>Strippers</deviceName>
    <manufacturerName>Aspen Surgical Products, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000008255</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C01901901</emdnCode>
    <emdnDescription>VEIN STRIPPER DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>78-2003</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:04:16.229Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663112197</udiDi>
    <basicUdiDi>08406631EZESITKX</basicUdiDi>
    <tradeName>Eze-Sit® Valvulotome</tradeName>
    <deviceName>Eze-Sit Valvulotome</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019017</emdnCode>
    <emdnDescription>VALVULOTOMES, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>TIVK2030M</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:36.192Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663112067</udiDi>
    <basicUdiDi>08406631TufTexOTWAL</basicUdiDi>
    <tradeName>TufTex® Over-the-Wire Embolectomy Catheter</tradeName>
    <deviceName>TufTex® Over-the-Wire Embolectomy Catheter</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019002</emdnCode>
    <emdnDescription>EMBOLECTOMY CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1651-34M</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:33.782Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663111831</udiDi>
    <basicUdiDi>08406631SyntelOTWQU</basicUdiDi>
    <tradeName>Syntel® Silicone Over-the-Wire Embolectomy Catheter</tradeName>
    <deviceName>Syntel® Silicone Over-the-Wire Embolectomy Catheter</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019002</emdnCode>
    <emdnDescription>EMBOLECTOMY CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>A4E01M</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:29.787Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663111749</udiDi>
    <basicUdiDi>08406631SyntelRTST</basicUdiDi>
    <tradeName>Syntel® Silicone Embolectomy Catheter - Regular Tip</tradeName>
    <deviceName>Syntel® Silicone Embolectomy Catheter - Regular Tip</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019002</emdnCode>
    <emdnDescription>EMBOLECTOMY CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1801-26M</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:28.972Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663111190</udiDi>
    <basicUdiDi>08406631TufTexSLE8</basicUdiDi>
    <tradeName>TufTex® Embolectomy Catheter</tradeName>
    <deviceName>TufTex Embolectomy Catheter</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019002</emdnCode>
    <emdnDescription>EMBOLECTOMY CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1601-24M</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:23.550Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663111169</udiDi>
    <basicUdiDi>08406631LMATVtomAV</basicUdiDi>
    <tradeName>LeMaitre Valvulotome</tradeName>
    <deviceName>LeMaitre® Valvulotome</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019017</emdnCode>
    <emdnDescription>VALVULOTOMES, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1009-00M</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:22.829Z</lastUpdated>
  </row>
  <row>
    <udiDi>00840663110469</udiDi>
    <basicUdiDi>08406631Chevalier3P</basicUdiDi>
    <tradeName>00840663110469</tradeName>
    <deviceName>Chevalier Valvulotome</deviceName>
    <manufacturerName>LeMaitre Vascular, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000016778</manufacturerSrn>
    <authorisedRepresentativeName>LeMaitre Vascular GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000013539</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019017</emdnCode>
    <emdnDescription>VALVULOTOMES, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>40025</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T02:01:21.005Z</lastUpdated>
  </row>
  <row>
    <udiDi>00827002583412</udiDi>
    <basicUdiDi>0827002CVI017FH</basicUdiDi>
    <tradeName>Pin Vise Polymer</tradeName>
    <deviceName>Pin Vise Polymer</deviceName>
    <manufacturerName>Cook Vandergrift Inc</manufacturerName>
    <manufacturerSrn>US-MF-000002657</manufacturerSrn>
    <authorisedRepresentativeName>COOK MEDICAL EUROPE LIMITED</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IE-AR-000000907</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C01901903</emdnCode>
    <emdnDescription>VESSEL HARVESTING SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LR-PVP001</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-16T01:47:11.363Z</lastUpdated>
  </row>
  <row>
    <udiDi>00813132029661</udiDi>
    <basicUdiDi>081313202BM888NE</basicUdiDi>
    <tradeName>LLD accessory kit</tradeName>
    <deviceName>LLD accessory kit</deviceName>
    <manufacturerName>Philips Image Guided Therapy Corporation</manufacturerName>
    <manufacturerSrn>US-MF-000018632</manufacturerSrn>
    <authorisedRepresentativeName>Philips Medical Systems Nederland B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000001422</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C01901903</emdnCode>
    <emdnDescription>VESSEL HARVESTING SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>518-027</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T01:17:00.103Z</lastUpdated>
  </row>
  <row>
    <udiDi>00813132029654</udiDi>
    <basicUdiDi>081313202BM887NC</basicUdiDi>
    <tradeName>LLD lead cutter</tradeName>
    <deviceName>LLD lead cutter</deviceName>
    <manufacturerName>Philips Image Guided Therapy Corporation</manufacturerName>
    <manufacturerSrn>US-MF-000018632</manufacturerSrn>
    <authorisedRepresentativeName>Philips Medical Systems Nederland B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000001422</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C01901903</emdnCode>
    <emdnDescription>VESSEL HARVESTING SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>518-024</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T01:16:59.283Z</lastUpdated>
  </row>
  <row>
    <udiDi>00813132029616</udiDi>
    <basicUdiDi>081313202BM399MS</basicUdiDi>
    <tradeName>LLD lead locking device</tradeName>
    <deviceName>LLD lead locking device</deviceName>
    <manufacturerName>Philips Image Guided Therapy Corporation</manufacturerName>
    <manufacturerSrn>US-MF-000018632</manufacturerSrn>
    <authorisedRepresentativeName>Philips Medical Systems Nederland B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000001422</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C01901903</emdnCode>
    <emdnDescription>VESSEL HARVESTING SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>518-021</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T01:16:58.494Z</lastUpdated>
  </row>
  <row>
    <udiDi>00810123710010</udiDi>
    <basicUdiDi>08101237142-102X9</basicUdiDi>
    <tradeName>ClotTriever BOLD Catheter</tradeName>
    <deviceName>ClotTriever BOLD Catheter</deviceName>
    <manufacturerName>Inari Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000008693</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019002</emdnCode>
    <emdnDescription>EMBOLECTOMY CATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>42-102</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:54:23.068Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000723293</udiDi>
    <basicUdiDi>0763000B00004067E</basicUdiDi>
    <tradeName>ClosureRFS™</tradeName>
    <deviceName>ClosureRFS Stylet</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0190190401</emdnCode>
    <emdnDescription>CATHETERS FOR RADIOFREQUENCY ENDOVENOUS ABLATION</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>RFS2-6-12</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:08:00.649Z</lastUpdated>
  </row>
  <row>
    <udiDi>00763000552169</udiDi>
    <basicUdiDi>0763000B00004057C</basicUdiDi>
    <tradeName>ClosureFast™</tradeName>
    <deviceName>ClosureFast Catheter</deviceName>
    <manufacturerName>Medtronic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000019977</manufacturerSrn>
    <authorisedRepresentativeName>Medtronic B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000006050</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0190190401</emdnCode>
    <emdnDescription>CATHETERS FOR RADIOFREQUENCY ENDOVENOUS ABLATION</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CF6-8-60</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T00:06:48.459Z</lastUpdated>
  </row>
  <row>
    <udiDi>00685447018711</udiDi>
    <basicUdiDi>06854470013PT</basicUdiDi>
    <tradeName>NRG™</tradeName>
    <deviceName>NRG RF Transseptal Kit</deviceName>
    <manufacturerName>Baylis Medical Company Inc.</manufacturerName>
    <manufacturerSrn>CA-PR-000047675</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019015</emdnCode>
    <emdnDescription>CARDIAC TRANSSEPTAL PUNCTURE KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>NTK3001</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-15T22:13:30.494Z</lastUpdated>
  </row>
  <row>
    <udiDi>00685447016571</udiDi>
    <basicUdiDi>06854470026Q4</basicUdiDi>
    <tradeName>VersaCross Connect™</tradeName>
    <deviceName>VersaCross Connect Access Solution</deviceName>
    <manufacturerName>Baylis Medical Company Inc.</manufacturerName>
    <manufacturerSrn>CA-PR-000047675</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019015</emdnCode>
    <emdnDescription>CARDIAC TRANSSEPTAL PUNCTURE KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>VXAK3003</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-15T22:13:30.451Z</lastUpdated>
  </row>
  <row>
    <udiDi>00685447009337</udiDi>
    <basicUdiDi>06854470015PX</basicUdiDi>
    <tradeName>VersaCross™</tradeName>
    <deviceName>VersaCross Steerable Access Solution</deviceName>
    <manufacturerName>Baylis Medical Company Inc.</manufacturerName>
    <manufacturerSrn>CA-PR-000047675</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019015</emdnCode>
    <emdnDescription>CARDIAC TRANSSEPTAL PUNCTURE KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>VSTK3003</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-15T22:13:28.902Z</lastUpdated>
  </row>
  <row>
    <udiDi>00685447008910</udiDi>
    <basicUdiDi>06854470014PV</basicUdiDi>
    <tradeName>VersaCross™</tradeName>
    <deviceName>VersaCross Access Solution</deviceName>
    <manufacturerName>Baylis Medical Company Inc.</manufacturerName>
    <manufacturerSrn>CA-PR-000047675</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C019015</emdnCode>
    <emdnDescription>CARDIAC TRANSSEPTAL PUNCTURE KITS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>VXSK3001</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-15T22:13:23.158Z</lastUpdated>
  </row>
</eudamedExport>