<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>89080246910018</udiDi>
    <basicUdiDi>890802469100185</basicUdiDi>
    <tradeName>AXIFLOW</tradeName>
    <deviceName>DBS CARD (Specimen Collection Card)</deviceName>
    <manufacturerName>AXIFLOW BIOTECH PRIVATE LIMITED</manufacturerName>
    <manufacturerSrn>IN-MF-000042655</manufacturerSrn>
    <authorisedRepresentativeName>Europecert UG (haftungsbeschränkt)</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000004974</authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf A</riskClass>
    <legislation>IVDR 2017/746</legislation>
    <emdnCode>W0501010199</emdnCode>
    <emdnDescription>VENOUS OR ARTERIOUS BLOOD COLLECTION DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>AXI-DBS-001</reference>
    <placedOnMarketCountry>Sweden</placedOnMarketCountry>
    <lastUpdated>2026-07-03T19:10:40.951Z</lastUpdated>
  </row>
</eudamedExport>