<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>08052275280009</udiDi>
    <basicUdiDi>80522752810100030055</basicUdiDi>
    <tradeName>dia-BRUXO System</tradeName>
    <deviceName>dia-BRUXO System: EMG Device</deviceName>
    <manufacturerName>Biotechnovations srl</manufacturerName>
    <manufacturerSrn>IT-MF-000051527</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12100401</emdnCode>
    <emdnDescription>ELECTROMYOGRAPHS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1-01-0003-00</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T06:16:39.959Z</lastUpdated>
  </row>
</eudamedExport>