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    <tradeName>FTN Fixture 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>
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    <udiDi>08800049309193</udiDi>
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    <tradeName>FTN Fixture Driver</tradeName>
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    <manufacturerName>DIO Corporation</manufacturerName>
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    <udiDi>08800049309216</udiDi>
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    <tradeName>FTN Fixture Driver</tradeName>
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    <manufacturerName>DIO Corporation</manufacturerName>
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    <udiDi>08800049475898</udiDi>
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    <tradeName>DIO Water Membrane Lifter</tradeName>
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    <manufacturerName>DIO Corporation</manufacturerName>
    <manufacturerSrn>KR-MF-000008515</manufacturerSrn>
    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
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    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
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    <lastUpdated>2026-07-02T03:32:01.875Z</lastUpdated>
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    <udiDi>08800049436974</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Screw Remove Tip</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>2026-07-02T03:32:01.588Z</lastUpdated>
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    <udiDi>08800049494905</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Transfer Impression Coping</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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    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
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    <lastUpdated>2026-07-01T19:45:00.479Z</lastUpdated>
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    <udiDi>08800049494912</udiDi>
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    <tradeName>UniCon Transfer Impression Coping</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>
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    <lastUpdated>2026-07-01T19:44:59.924Z</lastUpdated>
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    <udiDi>08800049494929</udiDi>
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    <tradeName>UniCon Transfer Impression Coping</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
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    <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>2026-07-01T19:44:59.696Z</lastUpdated>
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    <udiDi>08800049494936</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Transfer Impression Coping Screw</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>2026-07-01T19:44:59.267Z</lastUpdated>
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    <udiDi>08800049494943</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Transfer Impression Coping Screw</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>2026-07-01T19:44:58.833Z</lastUpdated>
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    <udiDi>08800049494950</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Transfer Impression Coping Screw</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>2026-07-01T19:44:56.261Z</lastUpdated>
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    <udiDi>08800049494967</udiDi>
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    <tradeName>UniCon Transfer Impression Coping Screw</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>2026-07-01T19:44:55.561Z</lastUpdated>
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    <udiDi>08800049495124</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Lab Analog</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>2026-07-01T19:44:35.851Z</lastUpdated>
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    <udiDi>08800049385258</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Abutment Lab Analog</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>2026-07-01T19:44:35.400Z</lastUpdated>
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    <udiDi>08800049385265</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Abutment Lab Analog</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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    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
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    <lastUpdated>2026-07-01T19:44:35.065Z</lastUpdated>
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    <udiDi>08800049385272</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Abutment Lab Analog</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
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    <authorisedRepresentativeName>AR Experts B.V.</authorisedRepresentativeName>
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    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
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    <lastUpdated>2026-07-01T19:44:34.812Z</lastUpdated>
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    <udiDi>08800049385289</udiDi>
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    <tradeName>UniCon Abutment Lab Analog</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
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    <emdnDescription>SURGICAL DENTAL DEVICES - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>DIO Implant System Product Catalog Ver 7.0 (KR)</reference>
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    <lastUpdated>2026-07-01T19:44:34.597Z</lastUpdated>
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    <tradeName>UniCon Abutment Lab Analog</tradeName>
    <deviceName></deviceName>
    <manufacturerName>DIO Corporation</manufacturerName>
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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>
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    <lastUpdated>2026-07-01T19:44:34.410Z</lastUpdated>
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    <tradeName>UniCon Abutment Lab Analog</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>
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    <lastUpdated>2026-07-01T19:44:34.286Z</lastUpdated>
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    <udiDi>08800049385319</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>UniCon Abutment Lab Analog</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>2026-07-01T19:44:33.894Z</lastUpdated>
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