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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
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    <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>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
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    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
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    <deviceStatus>Piyasada</deviceStatus>
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    <lastUpdated>2026-07-12T06:45:27.689Z</lastUpdated>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
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    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
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    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:45:26.891Z</lastUpdated>
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    <udiDi>D-80565185044574H</udiDi>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous half cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
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    <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>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
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    <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>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous half cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
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    <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>
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    <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>
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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous half cup</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
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    <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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    <udiDi>D-80565185043894R</udiDi>
    <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>
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    <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>
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    <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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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous block</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
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    <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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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous block</deviceName>
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    <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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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous block</deviceName>
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    <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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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous block</deviceName>
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    <authorisedRepresentativeName></authorisedRepresentativeName>
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    <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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    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous wedge</deviceName>
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    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
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    <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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    <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>
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