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<eudamedExport entity="devices">
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    <udiDi>08809447656090</udiDi>
    <basicUdiDi>88094476511202AVS</basicUdiDi>
    <tradeName>LaseMD Ultra Laser System main body (Including Fiber and Handpiece)</tradeName>
    <deviceName>Thulium laser</deviceName>
    <manufacturerName>Lutronic Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000009035</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12011099</emdnCode>
    <emdnDescription>LASER SURGERY INSTRUMENTS - OTHER</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>LaseMD Ultra</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:02:29.825Z</lastUpdated>
  </row>
  <row>
    <udiDi>08809447654713</udiDi>
    <basicUdiDi>88094476510118AVX</basicUdiDi>
    <tradeName>5mm-SD585</tradeName>
    <deviceName>Frequency Doubled Q-switched Nd-YAG Laser system</deviceName>
    <manufacturerName>Lutronic Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000009035</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12011017</emdnCode>
    <emdnDescription>NEODYMIUM SURGICAL LASER</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>HOLLYWOOD SPECTRA</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:02:13.897Z</lastUpdated>
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  <row>
    <udiDi>08809447653723</udiDi>
    <basicUdiDi>88094476511102AVK</basicUdiDi>
    <tradeName>CLARITY II (ICD Type)</tradeName>
    <deviceName>Long-pulsed Alexandrite + Nd:YAG Laser, Long-pulsed Alexandrite Laser</deviceName>
    <manufacturerName>Lutronic Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000009035</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12011019</emdnCode>
    <emdnDescription>MULTI–PLATFORM LASER</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>CLARITY II (ICD Type)</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:02:13.124Z</lastUpdated>
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    <udiDi>08809447652665</udiDi>
    <basicUdiDi>88094476510116AVR</basicUdiDi>
    <tradeName>O type tip (Small size)</tradeName>
    <deviceName>Long pulsed Nd:YAG Laser</deviceName>
    <manufacturerName>Lutronic Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000009035</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12011019</emdnCode>
    <emdnDescription>MULTI–PLATFORM LASER</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>DermaV</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:02:09.109Z</lastUpdated>
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    <udiDi>08809447652269</udiDi>
    <basicUdiDi>88094476511007AVT</basicUdiDi>
    <tradeName>G49D BOX (10EA)</tradeName>
    <deviceName>Electrosurgical Unit</deviceName>
    <manufacturerName>Lutronic Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000009035</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12010902</emdnCode>
    <emdnDescription>ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>LUTRONIC GENIUS</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:02:08.294Z</lastUpdated>
  </row>
  <row>
    <udiDi>08809447651675</udiDi>
    <basicUdiDi>88094476510704AWQ</basicUdiDi>
    <tradeName>HEAD-830nm/590nm</tradeName>
    <deviceName>Phototherapy Unit</deviceName>
    <manufacturerName>Lutronic Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000009035</manufacturerSrn>
    <authorisedRepresentativeName>Emergo Europe B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000116</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12040299</emdnCode>
    <emdnDescription>GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - OTHER</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>HEALITE II</reference>
    <placedOnMarketCountry>Netherlands</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:02:07.509Z</lastUpdated>
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  <row>
    <udiDi>08809240011058</udiDi>
    <basicUdiDi>880924001PRKNW</basicUdiDi>
    <tradeName>08809240011058</tradeName>
    <deviceName>Auto Ref-Keratometer</deviceName>
    <manufacturerName>POTEC Co., Ltd.</manufacturerName>
    <manufacturerSrn>KR-MF-000012281</manufacturerSrn>
    <authorisedRepresentativeName>MDSS GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005430</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12120199</emdnCode>
    <emdnDescription>OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>PRK-5000</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:01:05.927Z</lastUpdated>
  </row>
  <row>
    <udiDi>08809220580765</udiDi>
    <basicUdiDi>88092205843507Y</basicUdiDi>
    <tradeName>08809220580765</tradeName>
    <deviceName>DANA 3cc syringe</deviceName>
    <manufacturerName>SOOIL Development Co., Ltd.</manufacturerName>
    <manufacturerSrn>KR-MF-000008627</manufacturerSrn>
    <authorisedRepresentativeName>Medical Technology Promedt Consulting GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000085</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12030385</emdnCode>
    <emdnDescription>INFUSION INSTRUMENTS - CONSUMABLES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SD-300</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-31T21:01:02.014Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800271100100</udiDi>
    <basicUdiDi>88002711KN-0005H</basicUdiDi>
    <tradeName>BiLumiX® Gen.3</tradeName>
    <deviceName>Head Lamp</deviceName>
    <manufacturerName>ChoiceTech Co., Ltd.</manufacturerName>
    <manufacturerSrn>KR-MF-000044226</manufacturerSrn>
    <authorisedRepresentativeName>Europecert UG (haftungsbeschränkt)</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000004974</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z129004</emdnCode>
    <emdnDescription>LIGHT SOURCES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>Headlamp-Gen.3</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:59:28.728Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800184100006</udiDi>
    <basicUdiDi>8800184SPIRO54</basicUdiDi>
    <tradeName>08800184100006</tradeName>
    <deviceName>SPIRO LENIS</deviceName>
    <manufacturerName>JNBIO</manufacturerName>
    <manufacturerSrn>KR-MF-000042575</manufacturerSrn>
    <authorisedRepresentativeName>Javitech Consulting GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000045915</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12150101</emdnCode>
    <emdnDescription>CLINICAL/DIAGNOSTIC SPIROMETERS</emdnDescription>
    <deviceStatus>Artık piyasada değil</deviceStatus>
    <reference>PRD-LS-001</reference>
    <placedOnMarketCountry>Denmark</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:59:22.441Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800115200010</udiDi>
    <basicUdiDi>88001152H-0001PL</basicUdiDi>
    <tradeName>OK-Handpiece</tradeName>
    <deviceName>Low Speed Dental Handpiece, pneumatic</deviceName>
    <manufacturerName>Jaintek Co., Ltd.</manufacturerName>
    <manufacturerSrn>KR-MF-000045113</manufacturerSrn>
    <authorisedRepresentativeName>KTR Europe GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005685</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12110199</emdnCode>
    <emdnDescription>INSTRUMENTS FOR DENTAL TREATMENT UNITS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OKH4</reference>
    <placedOnMarketCountry>Poland</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:59:03.848Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800091150316</udiDi>
    <basicUdiDi>88000911nugabestN4AJ</basicUdiDi>
    <tradeName>08800091150316</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Nuga Medical Co., Ltd.</manufacturerName>
    <manufacturerSrn>KR-MF-000026434</manufacturerSrn>
    <authorisedRepresentativeName>KTR Europe GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000005685</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120622</emdnCode>
    <emdnDescription>MUSCLE STIMULATORS</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>N6-DM-13-02-000-01A-10</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:59:03.058Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800074500183</udiDi>
    <basicUdiDi>88000745VAAXT</basicUdiDi>
    <tradeName>View-M</tradeName>
    <deviceName>Self Vision Tester</deviceName>
    <manufacturerName>View-M Technology</manufacturerName>
    <manufacturerSrn>KR-MF-000010996</manufacturerSrn>
    <authorisedRepresentativeName>Obelis s.a.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000106</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12120180</emdnCode>
    <emdnDescription>OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS - HARDWARE ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>VAA-2000PS</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:58:58.262Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800074500008</udiDi>
    <basicUdiDi>88000745VLCYY</basicUdiDi>
    <tradeName>View-M</tradeName>
    <deviceName>Visual Chart System</deviceName>
    <manufacturerName>View-M Technology</manufacturerName>
    <manufacturerSrn>KR-MF-000010996</manufacturerSrn>
    <authorisedRepresentativeName>Obelis s.a.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>BE-AR-000000106</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12120180</emdnCode>
    <emdnDescription>OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS - HARDWARE ACCESSORIES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>VLC-1900</reference>
    <placedOnMarketCountry>Greece</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:58:57.487Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800069700154</udiDi>
    <basicUdiDi>88000697TapePatchHH</basicUdiDi>
    <tradeName>Tape Patch</tradeName>
    <deviceName>Tape Patch</deviceName>
    <manufacturerName>ATsens Co., Ltd.</manufacturerName>
    <manufacturerSrn>KR-MF-000017532</manufacturerSrn>
    <authorisedRepresentativeName>CMC Medical Devices &amp; Drugs SL</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>ES-AR-000000293</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12050485</emdnCode>
    <emdnDescription>HOLTER SYSTEM INSTRUMENTS FOR CARDIOVASCULAR PARAMETERS - CONSUMABLES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ATTPE-100</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:58:52.645Z</lastUpdated>
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    <udiDi>00877067000324</udiDi>
    <basicUdiDi>87706700FPRD-021UL</basicUdiDi>
    <tradeName>Dermadry - LARGE CASE</tradeName>
    <deviceName>Dermadry - Large Briefcase</deviceName>
    <manufacturerName>Dermadry Laboratories Inc.</manufacturerName>
    <manufacturerSrn>CA-MF-000025789</manufacturerSrn>
    <authorisedRepresentativeName>CEpartner4U</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000111</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120604</emdnCode>
    <emdnDescription>IONTOPHORESIS EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FPRD-021</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:57:28.640Z</lastUpdated>
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    <udiDi>00877067000300</udiDi>
    <basicUdiDi>87706700FPRD-019UZ</basicUdiDi>
    <tradeName>Dermadry - UNDERARM ELECTRODES</tradeName>
    <deviceName>Dermadry -Underarm electrodes</deviceName>
    <manufacturerName>Dermadry Laboratories Inc.</manufacturerName>
    <manufacturerSrn>CA-MF-000025789</manufacturerSrn>
    <authorisedRepresentativeName>CEpartner4U</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000111</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120604</emdnCode>
    <emdnDescription>IONTOPHORESIS EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FPRD-019</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:57:27.844Z</lastUpdated>
  </row>
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    <udiDi>00877067000294</udiDi>
    <basicUdiDi>87706700FPRD-018UX</basicUdiDi>
    <tradeName>Dermadry - TOWELS</tradeName>
    <deviceName>Dermadry -Towels</deviceName>
    <manufacturerName>Dermadry Laboratories Inc.</manufacturerName>
    <manufacturerSrn>CA-MF-000025789</manufacturerSrn>
    <authorisedRepresentativeName>CEpartner4U</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000111</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120604</emdnCode>
    <emdnDescription>IONTOPHORESIS EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FPRD-018</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:57:27.807Z</lastUpdated>
  </row>
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    <udiDi>00877067000287</udiDi>
    <basicUdiDi>87706700FPRD-017UV</basicUdiDi>
    <tradeName>Dermadry - HANDS &amp; FEET ELECTRODES</tradeName>
    <deviceName>Dermadry - Hands and Feet Electrodes</deviceName>
    <manufacturerName>Dermadry Laboratories Inc.</manufacturerName>
    <manufacturerSrn>CA-MF-000025789</manufacturerSrn>
    <authorisedRepresentativeName>CEpartner4U</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000111</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120604</emdnCode>
    <emdnDescription>IONTOPHORESIS EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FPRD-017</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:57:23.024Z</lastUpdated>
  </row>
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    <udiDi>00877067000256</udiDi>
    <basicUdiDi>87706700DERMADRY58</basicUdiDi>
    <tradeName>Dermadry - Total - EN/FR/DE/SP/IT/NL Europe</tradeName>
    <deviceName>Dermadry</deviceName>
    <manufacturerName>Dermadry Laboratories Inc.</manufacturerName>
    <manufacturerSrn>CA-MF-000025789</manufacturerSrn>
    <authorisedRepresentativeName>CEpartner4U</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000000111</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z120604</emdnCode>
    <emdnDescription>IONTOPHORESIS EQUIPMENT</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>FPRD-052</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-31T20:57:22.504Z</lastUpdated>
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</eudamedExport>