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    <tradeName>UniCon Solid Abutment Driver</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:30.870Z</lastUpdated>
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    <udiDi>08800049496121</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Solid Abutment Driver</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
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    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:16.785Z</lastUpdated>
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    <udiDi>08800049496091</udiDi>
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    <tradeName>UniCon Multi-Unit Abutment Driver</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
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    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:16.100Z</lastUpdated>
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    <udiDi>08800049385142</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
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    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:14.922Z</lastUpdated>
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    <udiDi>08800049385159</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:06.162Z</lastUpdated>
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    <udiDi>08800049385166</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:04.790Z</lastUpdated>
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    <udiDi>08800049385173</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:03.439Z</lastUpdated>
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    <udiDi>08800049385180</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:43:01.142Z</lastUpdated>
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    <udiDi>08800049385197</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:59.565Z</lastUpdated>
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    <udiDi>08800049385203</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:50.392Z</lastUpdated>
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    <udiDi>08800049385210</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:49.302Z</lastUpdated>
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    <udiDi>08800049385227</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:48.178Z</lastUpdated>
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    <udiDi>08800049385234</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:47.031Z</lastUpdated>
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    <udiDi>08800049385241</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Stopper (Sinus approach)</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:45.377Z</lastUpdated>
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    <udiDi>08800049488775</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Water Membrane Lifter</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:43.478Z</lastUpdated>
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    <udiDi>08800049488782</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Water Membrane Lifter</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
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    <riskClass>Sınıf I</riskClass>
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    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:34.461Z</lastUpdated>
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    <udiDi>08800049488942</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Sinus Membrane Detach tool</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:30.906Z</lastUpdated>
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    <udiDi>08800049490143</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Muliti-unit Selector Kit</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:42:20.500Z</lastUpdated>
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    <udiDi>08800049490068</udiDi>
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    <tradeName>Multi-unit Selector</tradeName>
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    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
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    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:41:58.063Z</lastUpdated>
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    <udiDi>08800049490075</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>Multi-unit Selector</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>NL-AR-000023989</authorisedRepresentativeSrn>
    <riskClass>Sınıf I</riskClass>
    <legislation>MDR 2017/745</legislation>
    <emdnCode>Q010399</emdnCode>
    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-07-02T19:41:57.253Z</lastUpdated>
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