<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>D-MA-1007-060033</udiDi>
    <basicUdiDi>B-MA-1007-060033</basicUdiDi>
    <tradeName>RENOVA iStim™ OAB2000</tradeName>
    <deviceName></deviceName>
    <manufacturerName>BlueWind Medical Ltd</manufacturerName>
    <manufacturerSrn>IL-MF-000009870</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>AIMDD</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription></emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>MA-1007-0600</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-15T22:58:22.653Z</lastUpdated>
  </row>
</eudamedExport>