<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
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    <udiDi>00850044054190</udiDi>
    <basicUdiDi>0850044054CDIWA</basicUdiDi>
    <tradeName>Nidra® Charge Dispersing Interface (CDI), Weekly</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Noctrix Health, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000051469</manufacturerSrn>
    <authorisedRepresentativeName>Obelis s.a.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000106</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062885</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - CONSUMABLES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CDI.30D.EU</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-10-08T06:11:56.874Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850044054176</udiDi>
    <basicUdiDi>0850044054CCGW3</basicUdiDi>
    <tradeName>Nidra® Compressive Conductive Garment (CCG), Large</tradeName>
    <deviceName>Nidra TOMAC Compressive Conductive Garment (CCG), Medium</deviceName>
    <manufacturerName>Noctrix Health, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000051469</manufacturerSrn>
    <authorisedRepresentativeName>Obelis s.a.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000106</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062799</emdnCode>
    <emdnDescription>FUNCTIONAL ELECTRICAL STIMULATION SYSTEMS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>NTX.CCGL150.EU</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-10-08T06:11:41.367Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850044054206</udiDi>
    <basicUdiDi>0850044054CDIWA</basicUdiDi>
    <tradeName>Nidra® Charge Dispersing Interface (CDI), Monthly</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Noctrix Health, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000051469</manufacturerSrn>
    <authorisedRepresentativeName>Obelis s.a.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000106</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062885</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - CONSUMABLES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CDI.08D.EU</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-10-01T19:46:18.959Z</lastUpdated>
  </row>
</eudamedExport>