<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>04270000054105</udiDi>
    <basicUdiDi>B-04270000054105</basicUdiDi>
    <tradeName>pRELAX - Vasospasm Treatment Device</tradeName>
    <deviceName>pRELAX - Vasospasm Treatment Device</deviceName>
    <manufacturerName>femtos GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000005499</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>C0104040299</emdnCode>
    <emdnDescription>NEUROVASCULAR ANGIOGRAPHY THERAPEUTIC DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>PRELAX-4-20</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-08-05T09:47:55.565Z</lastUpdated>
  </row>
</eudamedExport>