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    <basicUdiDi>426256HNJ-1000LQ</basicUdiDi>
    <tradeName>dres kegel</tradeName>
    <deviceName>Biofeedback System</deviceName>
    <manufacturerName>SmartMann GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000049779</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SMM-CA0508-2K504</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-31T02:43:38.629Z</lastUpdated>
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    <udiDi>04262560510030</udiDi>
    <basicUdiDi>426256HNJ-350KPK</basicUdiDi>
    <tradeName>dres kegel</tradeName>
    <deviceName>Biofeedback System</deviceName>
    <manufacturerName>SmartMann GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000049779</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SMM-CA0507-1K504</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-31T02:43:37.049Z</lastUpdated>
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    <udiDi>08056992331327</udiDi>
    <basicUdiDi>803377232CAT-U0703MW</basicUdiDi>
    <tradeName>Abdominal catheter with 1 balloon</tradeName>
    <deviceName>CATHETERS FOR PELVIC FLOOR BIOFEEDBACK EXERCISE</deviceName>
    <manufacturerName>Medica S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000025691</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1RB-12B1</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T05:16:20.401Z</lastUpdated>
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    <udiDi>08033638801116</udiDi>
    <basicUdiDi>803363880PLVRHABWY</basicUdiDi>
    <tradeName>FISIANAL</tradeName>
    <deviceName>Biofeedback</deviceName>
    <manufacturerName>SAPI MED S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000023733</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>B.0500</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-03T05:04:45.356Z</lastUpdated>
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    <udiDi>04262560510016</udiDi>
    <basicUdiDi>426256HNJ-7000N2</basicUdiDi>
    <tradeName>dres kegel</tradeName>
    <deviceName>Biofeedback System</deviceName>
    <manufacturerName>SmartMann GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000049779</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>SMM-CA0509-3K504</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-07-01T20:39:06.440Z</lastUpdated>
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    <udiDi>03770014642172</udiDi>
    <basicUdiDi>3770014642PER002V7</basicUdiDi>
    <tradeName>Perifit Care+</tradeName>
    <deviceName>Perifit Care+</deviceName>
    <manufacturerName>X6 Innovations</manufacturerName>
    <manufacturerSrn>FR-MF-000029894</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>PER002</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-01T12:56:55.921Z</lastUpdated>
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    <udiDi>03770014642110</udiDi>
    <basicUdiDi>3770014642PER001V5</basicUdiDi>
    <tradeName>Perifit Care</tradeName>
    <deviceName>Perifit Care</deviceName>
    <manufacturerName>X6 Innovations</manufacturerName>
    <manufacturerSrn>FR-MF-000029894</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>Pink</reference>
    <placedOnMarketCountry>France</placedOnMarketCountry>
    <lastUpdated>2026-07-01T12:56:39.063Z</lastUpdated>
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    <udiDi>03770014642141</udiDi>
    <basicUdiDi>3770014642PER001V5</basicUdiDi>
    <tradeName>Perifit Care</tradeName>
    <deviceName></deviceName>
    <manufacturerName>X6 Innovations</manufacturerName>
    <manufacturerSrn>FR-MF-000029894</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>Green</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-23T15:23:59.903Z</lastUpdated>
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    <udiDi>08056992331334</udiDi>
    <basicUdiDi>803377232CAT-U0703MW</basicUdiDi>
    <tradeName>Abdominal catheter with 2 balloons</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Medica S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000025691</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf IIa</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>U070301</emdnCode>
    <emdnDescription>PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>2RB-12B2</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-16T03:53:33.640Z</lastUpdated>
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