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    <basicUdiDi>B-80565185046003W</basicUdiDi>
    <tradeName>OSTEOPLANT® Flex</tradeName>
    <deviceName>OSTEOPLANT® Flex cortical sheet</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OTC-C4</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:54.112Z</lastUpdated>
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    <udiDi>D-80565185045944U</udiDi>
    <basicUdiDi>B-80565185045944U</basicUdiDi>
    <tradeName>OSTEOPLANT® Flex</tradeName>
    <deviceName>OSTEOPLANT® Flex cortical sheet</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OTC-C1</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:53.314Z</lastUpdated>
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    <udiDi>D-80565185045874X</udiDi>
    <basicUdiDi>B-80565185045874X</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous cortical stick</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-30</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:52.522Z</lastUpdated>
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    <udiDi>D-80565185045704E</udiDi>
    <basicUdiDi>B-80565185045704E</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous cortical stick</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-20B</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:50.908Z</lastUpdated>
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    <udiDi>D-80565185045634H</udiDi>
    <basicUdiDi>B-80565185045634H</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cortical rod</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-10</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:45.308Z</lastUpdated>
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    <udiDi>D-80565185045564L</udiDi>
    <basicUdiDi>B-80565185045564L</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cortical rod</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-09</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:44.506Z</lastUpdated>
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  <row>
    <udiDi>D-80565185045494P</udiDi>
    <basicUdiDi>B-80565185045494P</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cortical rod</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-08</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:43.709Z</lastUpdated>
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  <row>
    <udiDi>D-805651850453246</udiDi>
    <basicUdiDi>B-805651850453246</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous dihedron</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-07A</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:42.918Z</lastUpdated>
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  <row>
    <udiDi>D-805651850452549</udiDi>
    <basicUdiDi>B-805651850452549</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-075P</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:37.291Z</lastUpdated>
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    <udiDi>D-80565185045184C</udiDi>
    <basicUdiDi>B-80565185045184C</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Flex cancellous acetabular mat</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-070</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:36.489Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185045013T</udiDi>
    <basicUdiDi>B-80565185045013T</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900402</emdnCode>
    <emdnDescription>RESORBABLE FILLING AND RECONSTRUCTION DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-07</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:35.784Z</lastUpdated>
  </row>
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    <udiDi>D-80565185044954R</udiDi>
    <basicUdiDi>B-80565185044954R</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-06B</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:34.105Z</lastUpdated>
  </row>
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    <udiDi>D-80565185044884U</udiDi>
    <basicUdiDi>B-80565185044884U</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-06</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:28.492Z</lastUpdated>
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  <row>
    <udiDi>D-80565185044714B</udiDi>
    <basicUdiDi>B-80565185044714B</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-05B</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:27.689Z</lastUpdated>
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    <udiDi>D-80565185044644E</udiDi>
    <basicUdiDi>B-80565185044644E</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-05</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:26.891Z</lastUpdated>
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    <udiDi>D-80565185044574H</udiDi>
    <basicUdiDi>B-80565185044574H</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous half cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-0460A</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:26.090Z</lastUpdated>
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    <udiDi>D-80565185044403Y</udiDi>
    <basicUdiDi>B-80565185044403Y</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-0460</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:19.688Z</lastUpdated>
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    <udiDi>D-805651850443343</udiDi>
    <basicUdiDi>B-805651850443343</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous half cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-0456A</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:18.898Z</lastUpdated>
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    <udiDi>D-805651850442646</udiDi>
    <basicUdiDi>B-805651850442646</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-0456</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:17.281Z</lastUpdated>
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    <udiDi>D-805651850441949</udiDi>
    <basicUdiDi>B-805651850441949</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous half cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-0452A</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:16.480Z</lastUpdated>
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