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    <basicUdiDi>69517405ES02R3</basicUdiDi>
    <tradeName>TENS Therapy Device</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Shenzhen Jumper Medical Equipment Co.,Ltd</manufacturerName>
    <manufacturerSrn>CN-MF-000014343</manufacturerSrn>
    <authorisedRepresentativeName>MedPath GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000087</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>JPD-ES210</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-13T08:18:47.064Z</lastUpdated>
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    <udiDi>06951740550109</udiDi>
    <basicUdiDi>69517405ES02R3</basicUdiDi>
    <tradeName>TENS Therapy Device</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Shenzhen Jumper Medical Equipment Co.,Ltd</manufacturerName>
    <manufacturerSrn>CN-MF-000014343</manufacturerSrn>
    <authorisedRepresentativeName>MedPath GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000087</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>JPD-ES220</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-13T08:18:47.044Z</lastUpdated>
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    <udiDi>06951740550352</udiDi>
    <basicUdiDi>69517405ES02R3</basicUdiDi>
    <tradeName>TENS Therapy Device</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Shenzhen Jumper Medical Equipment Co.,Ltd</manufacturerName>
    <manufacturerSrn>CN-MF-000014343</manufacturerSrn>
    <authorisedRepresentativeName>MedPath GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000087</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>JPD-ES220</reference>
    <placedOnMarketCountry>Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-13T08:18:47.019Z</lastUpdated>
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    <udiDi>06951740550505</udiDi>
    <basicUdiDi>69517405ES02R3</basicUdiDi>
    <tradeName>Medicare</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Shenzhen Jumper Medical Equipment Co.,Ltd</manufacturerName>
    <manufacturerSrn>CN-MF-000014343</manufacturerSrn>
    <authorisedRepresentativeName>MedPath GmbH</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000000087</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>JPD-ES210</reference>
    <placedOnMarketCountry>Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-13T08:18:47.002Z</lastUpdated>
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    <udiDi>08437023265000</udiDi>
    <basicUdiDi>B-08437023265000</basicUdiDi>
    <tradeName>EPI® ALPHA</tradeName>
    <deviceName>EPI® ALPHA</deviceName>
    <manufacturerName>EPI ADVANCED MEDICINE S.L.</manufacturerName>
    <manufacturerSrn>ES-MF-000035622</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>EPI® ALPHA</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-07T22:01:21.123Z</lastUpdated>
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  <row>
    <udiDi>08055719580109</udiDi>
    <basicUdiDi>B-08055719580109</basicUdiDi>
    <tradeName>FIRING</tradeName>
    <deviceName>FIRING</deviceName>
    <manufacturerName>Project Blue Generation s.r.l.</manufacturerName>
    <manufacturerSrn>IT-MF-000027914</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIb</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>7F00</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-07T18:00:27.949Z</lastUpdated>
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    <udiDi>08437023158012</udiDi>
    <basicUdiDi>8437023158EPTEV02LQ</basicUdiDi>
    <tradeName>EPTE BIPOLAR System</tradeName>
    <deviceName>EPTE BIPOLAR</deviceName>
    <manufacturerName>IONCLINICS &amp; DEIONIC, S.L.</manufacturerName>
    <manufacturerSrn>ES-MF-000020207</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>EPTEV02DEV01</reference>
    <placedOnMarketCountry>Spain</placedOnMarketCountry>
    <lastUpdated>2026-07-03T12:12:10.644Z</lastUpdated>
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  <row>
    <udiDi>08053848210010</udiDi>
    <basicUdiDi>80538482120DM6E</basicUdiDi>
    <tradeName>Paingone Plus</tradeName>
    <deviceName>Paingone Plus</deviceName>
    <manufacturerName>ITALRES SRL</manufacturerName>
    <manufacturerSrn>IT-MF-000029584</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>20DM</reference>
    <placedOnMarketCountry>Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-03T06:53:53.011Z</lastUpdated>
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    <udiDi>08053848210003</udiDi>
    <basicUdiDi>80538482110DM,30DMX8</basicUdiDi>
    <tradeName>Paingone One</tradeName>
    <deviceName>Paingone One</deviceName>
    <manufacturerName>ITALRES SRL</manufacturerName>
    <manufacturerSrn>IT-MF-000029584</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>10DM</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-03T06:53:51.957Z</lastUpdated>
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  <row>
    <udiDi>07649990376066</udiDi>
    <basicUdiDi>7649990376DP006G8</basicUdiDi>
    <tradeName>MONOS</tradeName>
    <deviceName>MONOS</deviceName>
    <manufacturerName>AD SWISS MEDTECH SA</manufacturerName>
    <manufacturerSrn>CH-MF-000037918</manufacturerSrn>
    <authorisedRepresentativeName>DO WELL TECHNOLOGIES DI BUCCI CLAUDIA</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IT-AR-000029315</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DP006</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T03:51:39.337Z</lastUpdated>
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    <udiDi>07649990376059</udiDi>
    <basicUdiDi>7649990376DP005G6</basicUdiDi>
    <tradeName>07649990376059</tradeName>
    <deviceName>PONOS</deviceName>
    <manufacturerName>AD SWISS MEDTECH SA</manufacturerName>
    <manufacturerSrn>CH-MF-000037918</manufacturerSrn>
    <authorisedRepresentativeName>DO WELL TECHNOLOGIES DI BUCCI CLAUDIA</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IT-AR-000029315</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DP005</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T03:51:38.531Z</lastUpdated>
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    <udiDi>07649990376035</udiDi>
    <basicUdiDi>7649990376DP003G2</basicUdiDi>
    <tradeName>MERT</tradeName>
    <deviceName>MERT</deviceName>
    <manufacturerName>AD SWISS MEDTECH SA</manufacturerName>
    <manufacturerSrn>CH-MF-000037918</manufacturerSrn>
    <authorisedRepresentativeName>DO WELL TECHNOLOGIES DI BUCCI CLAUDIA</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IT-AR-000029315</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DP003</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T03:51:34.534Z</lastUpdated>
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    <udiDi>07649990376028</udiDi>
    <basicUdiDi>7649990376DP002FY</basicUdiDi>
    <tradeName>Vibra GO</tradeName>
    <deviceName>Vibra GO</deviceName>
    <manufacturerName>AD SWISS MEDTECH SA</manufacturerName>
    <manufacturerSrn>CH-MF-000037918</manufacturerSrn>
    <authorisedRepresentativeName>DO WELL TECHNOLOGIES DI BUCCI CLAUDIA</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IT-AR-000029315</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DP002</reference>
    <placedOnMarketCountry>Slovenia</placedOnMarketCountry>
    <lastUpdated>2026-07-03T03:51:19.295Z</lastUpdated>
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  <row>
    <udiDi>07649990376011</udiDi>
    <basicUdiDi>7649990376DP001FW</basicUdiDi>
    <tradeName>Vibra 3.0</tradeName>
    <deviceName>DP001 Vibra 3.0</deviceName>
    <manufacturerName>AD SWISS MEDTECH SA</manufacturerName>
    <manufacturerSrn>CH-MF-000037918</manufacturerSrn>
    <authorisedRepresentativeName>DO WELL TECHNOLOGIES DI BUCCI CLAUDIA</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>IT-AR-000029315</authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DP001</reference>
    <placedOnMarketCountry>Poland</placedOnMarketCountry>
    <lastUpdated>2026-07-03T03:51:18.496Z</lastUpdated>
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  <row>
    <udiDi>07350012440268</udiDi>
    <basicUdiDi>7350012440268SB</basicUdiDi>
    <tradeName>TetraHub</tradeName>
    <deviceName>TetraHub</deviceName>
    <manufacturerName>Senzime AB</manufacturerName>
    <manufacturerSrn>SE-MF-000016903</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SEN 2017</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:49:09.408Z</lastUpdated>
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    <udiDi>07350012440251</udiDi>
    <basicUdiDi>7350012440251RS</basicUdiDi>
    <tradeName>TetraSensitive</tradeName>
    <deviceName>TetraSensitive</deviceName>
    <manufacturerName>Senzime AB</manufacturerName>
    <manufacturerSrn>SE-MF-000016903</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SEN 2016</reference>
    <placedOnMarketCountry>Sweden</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:49:05.404Z</lastUpdated>
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    <udiDi>07350012440237</udiDi>
    <basicUdiDi>7350012440237RY</basicUdiDi>
    <tradeName>TetraGraph Monitor</tradeName>
    <deviceName>TetraGraph Monitor</deviceName>
    <manufacturerName>Senzime AB</manufacturerName>
    <manufacturerSrn>SE-MF-000016903</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>SEN 2015</reference>
    <placedOnMarketCountry>Northern Ireland</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:49:04.604Z</lastUpdated>
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    <udiDi>07350012440213</udiDi>
    <basicUdiDi>7350012440213RJ</basicUdiDi>
    <tradeName>TetraSensitive</tradeName>
    <deviceName>TetraSensitive</deviceName>
    <manufacturerName>Senzime AB</manufacturerName>
    <manufacturerSrn>SE-MF-000016903</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SEN 2014</reference>
    <placedOnMarketCountry>Sweden</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:49:03.825Z</lastUpdated>
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    <udiDi>07350012440190</udiDi>
    <basicUdiDi>7350012440190RX</basicUdiDi>
    <tradeName>TetraSens Pediatric</tradeName>
    <deviceName>TetraSens, Pediatric</deviceName>
    <manufacturerName>Senzime AB</manufacturerName>
    <manufacturerSrn>SE-MF-000016903</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SEN 2013</reference>
    <placedOnMarketCountry>Sweden</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:49:03.021Z</lastUpdated>
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    <udiDi>07350012440176</udiDi>
    <basicUdiDi>7350012440176S5</basicUdiDi>
    <tradeName>TetraSens Electrode</tradeName>
    <deviceName>TetraSens</deviceName>
    <manufacturerName>Senzime AB</manufacturerName>
    <manufacturerSrn>SE-MF-000016903</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Z12062899</emdnCode>
    <emdnDescription>NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SEN 2012</reference>
    <placedOnMarketCountry>Sweden</placedOnMarketCountry>
    <lastUpdated>2026-07-03T01:48:59.021Z</lastUpdated>
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