<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>05063000000314</udiDi>
    <basicUdiDi>50630003DH/C1YB</basicUdiDi>
    <tradeName>05063000000314</tradeName>
    <deviceName>Hot &amp; Cold Therapy Disc</deviceName>
    <manufacturerName>Neo G Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000004603</manufacturerSrn>
    <authorisedRepresentativeName>European Healthcare &amp; Device Solutions Ltd.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IE-AR-000003999</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120602</emdnCode>
    <emdnDescription>PHYSIOTHERAPY EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>3DH/C1</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-31T06:09:12.033Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060758940015</udiDi>
    <basicUdiDi>506075894EHTKDG</basicUdiDi>
    <tradeName>eXroid Haemorrhoid Treatment Kit</tradeName>
    <deviceName>eXroid Haemorrhoid Treatment Kit</deviceName>
    <manufacturerName>eXroid Technology Ltd</manufacturerName>
    <manufacturerSrn>GB-MF-000012828</manufacturerSrn>
    <authorisedRepresentativeName>Advena Limited</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>MT-AR-000000234</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120601</emdnCode>
    <emdnDescription>ELECTROTHERAPY EQUIPMENT (INCLUDED TENS)</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>EXR105</reference>
    <placedOnMarketCountry>Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:53:45.070Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060758940008</udiDi>
    <basicUdiDi>506075894EHTS1.2JD</basicUdiDi>
    <tradeName>eXroid Haemorrhoid Treatment Device</tradeName>
    <deviceName>eXroid Haemorrhoid Treatment Device</deviceName>
    <manufacturerName>eXroid Technology Ltd</manufacturerName>
    <manufacturerSrn>GB-MF-000012828</manufacturerSrn>
    <authorisedRepresentativeName>Advena Limited</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>MT-AR-000000234</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120601</emdnCode>
    <emdnDescription>ELECTROTHERAPY EQUIPMENT (INCLUDED TENS)</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>EXR101-104</reference>
    <placedOnMarketCountry>Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:53:44.368Z</lastUpdated>
  </row>
  <row>
    <udiDi>05055982788977</udiDi>
    <basicUdiDi>5060693520013VG</basicUdiDi>
    <tradeName>FLOWTRON</tradeName>
    <deviceName>ACS900 PUMP UK STD TUBE SET</deviceName>
    <manufacturerName>ArjoHuntleigh AB</manufacturerName>
    <manufacturerSrn>SE-MF-000000696</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120607</emdnCode>
    <emdnDescription>PNEUMATIC COMPRESSION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>526000-29</reference>
    <placedOnMarketCountry>Bulgaria</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:51:43.302Z</lastUpdated>
  </row>
  <row>
    <udiDi>05055982788335</udiDi>
    <basicUdiDi>5060693520228W7</basicUdiDi>
    <tradeName>Sara Combilizer</tradeName>
    <deviceName>SARA COMBILIZER</deviceName>
    <manufacturerName>ArjoHuntleigh AB</manufacturerName>
    <manufacturerSrn>SE-MF-000000696</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120616</emdnCode>
    <emdnDescription>ELECTROMECHANICAL SYSTEMS FOR PHYSICAL THERAPY</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>APA1000-BE</reference>
    <placedOnMarketCountry>Belgium</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:51:40.904Z</lastUpdated>
  </row>
  <row>
    <udiDi>05055982786348</udiDi>
    <basicUdiDi>5060693520129W4</basicUdiDi>
    <tradeName>Flowtron - DVT</tradeName>
    <deviceName>Intermittent Pressure Compression Limb Garment</deviceName>
    <manufacturerName>ArjoHuntleigh AB</manufacturerName>
    <manufacturerSrn>SE-MF-000000696</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120607</emdnCode>
    <emdnDescription>PNEUMATIC COMPRESSION EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DVT5</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:51:27.282Z</lastUpdated>
  </row>
  <row>
    <udiDi>05055982759199</udiDi>
    <basicUdiDi>5060693520105VN</basicUdiDi>
    <tradeName>Kwiktrak</tradeName>
    <deviceName>Maxi Sky 2</deviceName>
    <manufacturerName>ArjoHuntleigh AB</manufacturerName>
    <manufacturerSrn>SE-MF-000000696</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12069001</emdnCode>
    <emdnDescription>ELECTRIC HOISTS AND WALKERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>200-12825</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:51:15.401Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060481690607</udiDi>
    <basicUdiDi>506048169DataAcqProdAD</basicUdiDi>
    <tradeName>DG2 Wireless Dongle</tradeName>
    <deviceName>Data Acquisition Products</deviceName>
    <manufacturerName>Biometrics Ltd</manufacturerName>
    <manufacturerSrn>GB-MF-000002774</manufacturerSrn>
    <authorisedRepresentativeName>Advena Limited</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>MT-AR-000000234</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120617</emdnCode>
    <emdnDescription>MOVEMENT ANALYSIS INTEGRATED SYSTEMS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DG2 DataLITE PIONEER</reference>
    <placedOnMarketCountry>Malta</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:47:46.818Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060229532411</udiDi>
    <basicUdiDi>50602295300464</basicUdiDi>
    <tradeName>D25 Alpha Branding Iron Coil</tradeName>
    <deviceName>D25mm Alpha (Coated) Branding Iron Coil</deviceName>
    <manufacturerName>The Magstim Company Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000003956</manufacturerSrn>
    <authorisedRepresentativeName>Technomed Europe</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000002048</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120606</emdnCode>
    <emdnDescription>MAGNETOTHERAPY EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>5220-00</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:35:03.732Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060229530868</udiDi>
    <basicUdiDi>50602295300362</basicUdiDi>
    <tradeName>D70mm Air Film SHAM Coil</tradeName>
    <deviceName>Double 70mm Placebo Air Film Coil</deviceName>
    <manufacturerName>The Magstim Company Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000003956</manufacturerSrn>
    <authorisedRepresentativeName>Technomed Europe</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000002048</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120606</emdnCode>
    <emdnDescription>MAGNETOTHERAPY EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>3950-00</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:34:58.124Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060225390176</udiDi>
    <basicUdiDi>506022539ARDOOH01HR</basicUdiDi>
    <tradeName>Ardoo</tradeName>
    <deviceName>Ardoo Caresafe 140 Hoist</deviceName>
    <manufacturerName>Polymorit Ltd</manufacturerName>
    <manufacturerSrn>GB-MF-000024688</manufacturerSrn>
    <authorisedRepresentativeName>Eurolink Europe Compliance Limited</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IE-AR-000002852</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12069001</emdnCode>
    <emdnDescription>ELECTRIC HOISTS AND WALKERS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ACHO001</reference>
    <placedOnMarketCountry>Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:34:51.368Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073978779</udiDi>
    <basicUdiDi>506007397OPH400A89</basicUdiDi>
    <tradeName>Kegel8®</tradeName>
    <deviceName>Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>AB pazarı için değil</deviceStatus>
    <reference>OPH400A</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:55.056Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970575</udiDi>
    <basicUdiDi>506007397ECS831XP</basicUdiDi>
    <tradeName>NeuroTrac® Primera</tradeName>
    <deviceName>Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ECS831</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:54.257Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970551</udiDi>
    <basicUdiDi>506007397OPH2024R</basicUdiDi>
    <tradeName>Kegel8® Ultra 20</tradeName>
    <deviceName>Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OPH202</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:52.658Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970537</udiDi>
    <basicUdiDi>506007397OPH22555</basicUdiDi>
    <tradeName>Kegel8® V for Men</tradeName>
    <deviceName>Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OPH225</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:50.259Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970520</udiDi>
    <basicUdiDi>506007397OPH120P8U</basicUdiDi>
    <tradeName>Kegel8® MultiTone</tradeName>
    <deviceName>Neuromuscular Electrical stimulator system with EMG of physiotherapy, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OPH120P</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:48.656Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970513</udiDi>
    <basicUdiDi>506007397OPH3104V</basicUdiDi>
    <tradeName>Kegel8® Mother Nurture</tradeName>
    <deviceName>Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OPH310</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:47.866Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970346</udiDi>
    <basicUdiDi>506007397MYO120PDU</basicUdiDi>
    <tradeName>NeuroTrac® MyoPlus Pro</tradeName>
    <deviceName>Neuromuscular Electrical stimulator system with EMG of physiotherapy, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>MYO120P</reference>
    <placedOnMarketCountry>Norway</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:46.259Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970308</udiDi>
    <basicUdiDi>506007397MYO24PAR</basicUdiDi>
    <tradeName>NeuroTrac® MyoPlus2 Pro</tradeName>
    <deviceName>Neuromuscular Electrical stimulator system with EMG of physiotherapy, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>MYO220P</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:43.875Z</lastUpdated>
  </row>
  <row>
    <udiDi>05060073970292</udiDi>
    <basicUdiDi>506007397ECS305AZL</basicUdiDi>
    <tradeName>NeuroTrac® REHAB</tradeName>
    <deviceName>Neuromuscular electrical stimulator (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS) unit, battery powered</deviceName>
    <manufacturerName>Verity Medical Ltd.</manufacturerName>
    <manufacturerSrn>IE-MF-000007426</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ECS305A</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T05:26:16.427Z</lastUpdated>
  </row>
</eudamedExport>