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    <basicUdiDi>B-80565185043894R</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-03</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:13.104Z</lastUpdated>
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    <udiDi>D-80565185044023Q</udiDi>
    <basicUdiDi>B-80565185044023Q</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-0452</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:12.162Z</lastUpdated>
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    <udiDi>D-80565185043964N</udiDi>
    <basicUdiDi>B-80565185043964N</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Hemi femural-head</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-04</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:11.475Z</lastUpdated>
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    <udiDi>D-805651850437248</udiDi>
    <basicUdiDi>B-805651850437248</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-02B</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:11.383Z</lastUpdated>
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    <udiDi>D-80565185043654B</udiDi>
    <basicUdiDi>B-80565185043654B</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-02</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:53.217Z</lastUpdated>
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    <udiDi>D-80565185043584E</udiDi>
    <basicUdiDi>B-80565185043584E</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-01B2</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:52.418Z</lastUpdated>
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    <udiDi>D-80565185043413V</udiDi>
    <basicUdiDi>B-80565185043413V</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-01B</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:50.822Z</lastUpdated>
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    <udiDi>D-80565185043343Y</udiDi>
    <basicUdiDi>B-80565185043343Y</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-01A</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:48.407Z</lastUpdated>
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    <udiDi>D-805651850432743</udiDi>
    <basicUdiDi>B-805651850432743</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-0125P</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:46.917Z</lastUpdated>
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    <udiDi>D-80565185043033M</udiDi>
    <basicUdiDi>B-80565185043033M</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OSP-01</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:46.882Z</lastUpdated>
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    <udiDi>D-80565185043103J</udiDi>
    <basicUdiDi>B-80565185043103J</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-010P</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:46.879Z</lastUpdated>
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  <row>
    <udiDi>D-80565185042974K</udiDi>
    <basicUdiDi>B-80565185042974K</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Bone block for glena</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>OMC-80</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:44.122Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850428042</udiDi>
    <basicUdiDi>B-805651850428042</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® 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>OMC-50b1</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:40.406Z</lastUpdated>
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  <row>
    <udiDi>D-805651850427345</udiDi>
    <basicUdiDi>B-805651850427345</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous dowel</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>OMC-15d</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:39.565Z</lastUpdated>
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    <udiDi>D-805651850426648</udiDi>
    <basicUdiDi>B-805651850426648</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Flex cancellous disk</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>OMC-05S</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:39.494Z</lastUpdated>
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    <udiDi>D-80565185042594B</udiDi>
    <basicUdiDi>B-80565185042594B</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous dowel</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>OMC-05</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:39.457Z</lastUpdated>
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    <udiDi>D-80565185042423S</udiDi>
    <basicUdiDi>B-80565185042423S</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous dowel</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>OMC-04</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:33.704Z</lastUpdated>
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    <udiDi>D-80565185042353V</udiDi>
    <basicUdiDi>B-80565185042353V</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous dowel</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>OMC-03</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:31.289Z</lastUpdated>
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    <udiDi>D-80565185042283Y</udiDi>
    <basicUdiDi>B-80565185042283Y</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM granules</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-AC5n</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:29.685Z</lastUpdated>
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    <udiDi>D-80565185042113F</udiDi>
    <basicUdiDi>B-80565185042113F</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM granules</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-AC20</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:44:28.086Z</lastUpdated>
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