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<eudamedExport entity="devices">
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    <udiDi>00850025525602</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Wingman</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription></emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>WGM35090CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-07T19:40:30.862Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525619</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Wingman</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription></emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>WGM35135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-07T19:40:08.089Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525282</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SPN35050CE</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T12:30:38.683Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525183</udiDi>
    <basicUdiDi>0850025525BSPURTX</basicUdiDi>
    <tradeName>Spur</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BSPUR460135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.866Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525190</udiDi>
    <basicUdiDi>0850025525BSPURTX</basicUdiDi>
    <tradeName>Spur</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BSPUR365135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.850Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525268</udiDi>
    <basicUdiDi>0850025525BSPURTX</basicUdiDi>
    <tradeName>Spur</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>AB pazarı için değil</deviceStatus>
    <reference>BSPUR365150CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.838Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525275</udiDi>
    <basicUdiDi>0850025525BSPURTX</basicUdiDi>
    <tradeName>Spur</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>PERIPHERAL ATHERECTOMY SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>AB pazarı için değil</deviceStatus>
    <reference>BSPUR460150CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.821Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525299</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SPN35090CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.780Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525305</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SPN35135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.754Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525312</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SPN35150CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.734Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525329</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP35090CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.714Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525336</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP35135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.692Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525343</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP35150CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.671Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525350</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP18090CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.646Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525367</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP18135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.626Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525374</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP18150CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.605Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525381</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP14090CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.582Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525398</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP14135CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.561Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850025525404</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Spex LP</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SLP14150CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T22:45:44.540Z</lastUpdated>
  </row>
  <row>
    <udiDi>00856492005005</udiDi>
    <basicUdiDi>856492005SupportCathKP</basicUdiDi>
    <tradeName>Wingman</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Reflow Medical, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000017521</manufacturerSrn>
    <authorisedRepresentativeName>MediMark Europe Sarl.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>FR-AR-000000182</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>C0104020202</emdnCode>
    <emdnDescription>PERIPHERAL EMBOLISATION CATHETERS AND MICROCATHETERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>WGM35065CE</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T20:18:17.682Z</lastUpdated>
  </row>
</eudamedExport>