<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
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    <udiDi>00850008595042</udiDi>
    <basicUdiDi>0850008595ECBZF</basicUdiDi>
    <tradeName>Exhaust Collection Bag</tradeName>
    <deviceName>Exhaust Collection Bag</deviceName>
    <manufacturerName>Channel Medsystems, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000028229</manufacturerSrn>
    <authorisedRepresentativeName>MedEnvoy Global BV</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000024028</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12080201</emdnCode>
    <emdnDescription>ENDOMETRIAL ABLATION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FGS-7015</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T03:09:51.938Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850008595035</udiDi>
    <basicUdiDi>0850008595CCDZ9</basicUdiDi>
    <tradeName>Cerene Cryotherapy Device</tradeName>
    <deviceName>Cerene Cryotherapy Device</deviceName>
    <manufacturerName>Channel Medsystems, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000028229</manufacturerSrn>
    <authorisedRepresentativeName>MedEnvoy Global BV</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000024028</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12080201</emdnCode>
    <emdnDescription>ENDOMETRIAL ABLATION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FGS-7000</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-16T03:09:51.098Z</lastUpdated>
  </row>
  <row>
    <udiDi>00850044503308</udiDi>
    <basicUdiDi>B-00850044503308</basicUdiDi>
    <tradeName>Minitouch</tradeName>
    <deviceName>Minitouch Generator</deviceName>
    <manufacturerName>MicroCube LLC</manufacturerName>
    <manufacturerSrn>US-MF-000043248</manufacturerSrn>
    <authorisedRepresentativeName>MPS Medical Product Service GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005009</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>Z12080201</emdnCode>
    <emdnDescription>ENDOMETRIAL ABLATION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>10001-01</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-05T08:02:48.923Z</lastUpdated>
  </row>
  <row>
    <udiDi>15420045508224</udiDi>
    <basicUdiDi>54200455GSSNOVASURENSE6</basicUdiDi>
    <tradeName>NovaSure Impedance Controlled Endometrial Ablation System Advanced Disposable Device</tradeName>
    <deviceName>NovaSure Impedance Controlled Endometrial Ablation System</deviceName>
    <manufacturerName>Hologic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000003310</manufacturerSrn>
    <authorisedRepresentativeName>Hologic BV</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000127</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12080201</emdnCode>
    <emdnDescription>ENDOMETRIAL ABLATION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>NS2013</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-02T01:05:53.286Z</lastUpdated>
  </row>
  <row>
    <udiDi>15420045508187</udiDi>
    <basicUdiDi>54200455GSSNOVASURERFCSJ</basicUdiDi>
    <tradeName>NovaSure Impedance Controlled Endometrial Ablation System RF Controller Model 10</tradeName>
    <deviceName>NovaSure Impedance Controlled Endometrial Ablation System</deviceName>
    <manufacturerName>Hologic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000003310</manufacturerSrn>
    <authorisedRepresentativeName>Hologic BV</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000127</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12080201</emdnCode>
    <emdnDescription>ENDOMETRIAL ABLATION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>RFC2010</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-02T01:05:52.492Z</lastUpdated>
  </row>
  <row>
    <udiDi>15420045515154</udiDi>
    <basicUdiDi>54200455GSSNOVASURENSE6</basicUdiDi>
    <tradeName>NovaSure Impedance Controlled Endometrial Ablation System V5 Disposable Device</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Hologic, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000003310</manufacturerSrn>
    <authorisedRepresentativeName>Hologic BV</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000127</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12080201</emdnCode>
    <emdnDescription>ENDOMETRIAL ABLATION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>NSV5-001</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-29T10:22:16.367Z</lastUpdated>
  </row>
</eudamedExport>