<?xml version="1.0" encoding="UTF-8"?>
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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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    <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>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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