<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>D-80565185030093B</udiDi>
    <basicUdiDi>B-80565185030093B</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous block</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>BGB-11</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:20.036Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185029274K</udiDi>
    <basicUdiDi>B-80565185029274K</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Cancellous cortical mix gel</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-OX23</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:18.446Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850291042</udiDi>
    <basicUdiDi>B-805651850291042</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Cancellous cortical mix gel</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-OX22n</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:16.836Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850290345</udiDi>
    <basicUdiDi>B-805651850290345</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Cancellous cortical mix gel</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-OX21n</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:14.434Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185028113X</udiDi>
    <basicUdiDi>B-80565185028113X</basicUdiDi>
    <tradeName>OSTEOPLANT® ANGIOSTAD</tradeName>
    <deviceName>OSTEOPLANT® ANGIOSTAD DBM gel</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>OGS-GEL2</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:12.824Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850280442</udiDi>
    <basicUdiDi>B-805651850280442</basicUdiDi>
    <tradeName>OSTEOPLANT® ANGIOSTAD</tradeName>
    <deviceName>OSTEOPLANT® ANGIOSTAD DBM gel</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>OGS-GEL1n</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:12.028Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027984Y</udiDi>
    <basicUdiDi>B-80565185027984Y</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM601</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:10.427Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027814F</udiDi>
    <basicUdiDi>B-80565185027814F</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM501</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:08.032Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027744J</udiDi>
    <basicUdiDi>B-80565185027744J</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM5</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:06.423Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027674M</udiDi>
    <basicUdiDi>B-80565185027674M</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM40</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:05.618Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850275044</udiDi>
    <basicUdiDi>B-805651850275044</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM2</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:03.220Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850274347</udiDi>
    <basicUdiDi>B-805651850274347</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM10</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:40:00.818Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027294D</udiDi>
    <basicUdiDi>B-80565185027294D</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM injectable paste</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>OGS-ACI5</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:59.214Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027123U</udiDi>
    <basicUdiDi>B-80565185027123U</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM injectable paste</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>OGS-ACI2</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:58.520Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027364A</udiDi>
    <basicUdiDi>B-80565185027364A</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</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>OGS-ACM1</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:56.120Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185027053X</udiDi>
    <basicUdiDi>B-80565185027053X</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM injectable paste</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>OGS-ACI10</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:42.363Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850263747</udiDi>
    <basicUdiDi>B-805651850263747</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous dry paste putty</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>BGP-05</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:37.550Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185026203N</udiDi>
    <basicUdiDi>B-80565185026203N</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous dry paste putty</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>BGP-03</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:36.743Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185026133R</udiDi>
    <basicUdiDi>B-80565185026133R</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous dry paste putty</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>BGP-02</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:35.958Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185026063U</udiDi>
    <basicUdiDi>B-80565185026063U</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous dry paste putty</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>BGP-01s</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:39:35.157Z</lastUpdated>
  </row>
</eudamedExport>