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<eudamedExport entity="devices">
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    <udiDi>08800049490112</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>2026-07-02T19:41:52.717Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049490129</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>2026-07-02T19:41:51.911Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049490136</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>2026-07-02T19:41:51.410Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049437322</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Fixture Driver(Ratchet)</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>2026-07-02T03:32:42.854Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049437339</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Fixture Driver(Ratchet)</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>2026-07-02T03:32:26.949Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049476529</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Multiunit 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>2026-07-02T03:32:26.844Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049476536</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Multiunit 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>2026-07-02T03:32:05.821Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049307984</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Abutment Removing 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>2026-07-02T03:32:05.484Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049480304</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIOnavi. Implant Connector</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>2026-07-02T03:32:05.252Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049480311</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIOnavi. Implant Connector</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>2026-07-02T03:32:04.865Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049302354</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO Ratchet Wrench</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>2026-07-02T03:32:04.365Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049308998</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <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>
    <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>2026-07-02T03:32:04.015Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049309018</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <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>
    <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>2026-07-02T03:32:03.402Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049309063</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <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>
    <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>2026-07-02T03:32:03.079Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049309087</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <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>
    <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>2026-07-02T03:32:02.701Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049309193</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <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>
    <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>2026-07-02T03:32:02.494Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049309216</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <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>
    <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>2026-07-02T03:32:02.076Z</lastUpdated>
  </row>
  <row>
    <udiDi>08800049475898</udiDi>
    <basicUdiDi>880004921003A8</basicUdiDi>
    <tradeName>DIO 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>2026-07-02T03:32:01.875Z</lastUpdated>
  </row>
  <row>
    <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>
    <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>2026-07-02T03:32:01.588Z</lastUpdated>
  </row>
  <row>
    <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>
    <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>2026-07-01T19:45:00.479Z</lastUpdated>
  </row>
</eudamedExport>