<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>00850001105057</udiDi>
    <basicUdiDi>B-00850001105057</basicUdiDi>
    <tradeName>00850001105057</tradeName>
    <deviceName>ER-REBOA™ PLUS Catheter</deviceName>
    <manufacturerName>Prytime Medical Devices Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000008225</manufacturerSrn>
    <authorisedRepresentativeName>MPS Medical Product Service GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005009</authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>C019009</emdnCode>
    <emdnDescription>AORTIC OCCLUSION SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ER7232PLUS-EU</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-05T07:51:08.731Z</lastUpdated>
  </row>
  <row>
    <udiDi>00863092000132</udiDi>
    <basicUdiDi>08630920001KT1835ES6</basicUdiDi>
    <tradeName>00863092000132</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Prytime Medical Devices Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000008225</manufacturerSrn>
    <authorisedRepresentativeName>MPS Medical Product Service GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005009</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>ARTERIAL INTRODUCTION SETS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>KT1835E</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-21T20:15:25.506Z</lastUpdated>
  </row>
</eudamedExport>