<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>05056143201625</udiDi>
    <basicUdiDi>50561432BREELIBDP</basicUdiDi>
    <tradeName>Breelib</tradeName>
    <deviceName>Breelib Inhalation System</deviceName>
    <manufacturerName>Vectura Group Ltd</manufacturerName>
    <manufacturerSrn>GB-MF-000029993</manufacturerSrn>
    <authorisedRepresentativeName>Vectura Ireland Limited</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IE-AR-000026036</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12040210</emdnCode>
    <emdnDescription>ULTRASONIC NEBULISERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>08CD1042</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-01T22:51:35.334Z</lastUpdated>
  </row>
</eudamedExport>