<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>00860006094201</udiDi>
    <basicUdiDi>8600060942LLD4</basicUdiDi>
    <tradeName>LevaLap</tradeName>
    <deviceName>LevaLap Laparoscopic Access Device</deviceName>
    <manufacturerName>Core Access Surgical Technologies, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000033149</manufacturerSrn>
    <authorisedRepresentativeName>MedNet EC-REP GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000002</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>V9012</emdnCode>
    <emdnDescription>NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DMT-001</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-03T14:01:18.510Z</lastUpdated>
  </row>
</eudamedExport>