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    <tradeName>Del(7q) Deletion Probe</tradeName>
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    <manufacturerName>Cytocell Limited</manufacturerName>
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    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
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    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <tradeName>XCE 8 orange</tradeName>
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    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
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    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <deviceStatus>Piyasada</deviceStatus>
    <reference>D-0812-050-FI</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-26T20:56:40.313Z</lastUpdated>
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    <udiDi>04251315813120</udiDi>
    <basicUdiDi>42513158D-0812IVDJ8</basicUdiDi>
    <tradeName>XCE 12 orange</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf C</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>D-0812-050-OR</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-26T20:56:40.300Z</lastUpdated>
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    <udiDi>08906213930191</udiDi>
    <basicUdiDi>8906213933B1251CKUK</basicUdiDi>
    <tradeName>TRUPCR® BCR-ABL1 Control Kit</tradeName>
    <deviceName></deviceName>
    <manufacturerName>3B BlackBio Dx Limited</manufacturerName>
    <manufacturerSrn>IN-MF-000023698</manufacturerSrn>
    <authorisedRepresentativeName>Wellkang Ltd</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>XI-AR-000001836</authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf C</riskClass>
    <legislation>IVDR 2017/746</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>3B1252CK</reference>
    <placedOnMarketCountry></placedOnMarketCountry>
    <lastUpdated>2026-06-22T19:45:01.351Z</lastUpdated>
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    <basicUdiDi>5713915PP004TK</basicUdiDi>
    <tradeName>PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay</tradeName>
    <deviceName></deviceName>
    <manufacturerName>PentaBase A/S</manufacturerName>
    <manufacturerSrn>DK-MF-000023157</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf C</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>1849</reference>
    <placedOnMarketCountry>Denmark</placedOnMarketCountry>
    <lastUpdated>2026-06-20T23:33:19.489Z</lastUpdated>
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    <tradeName>PlentiPlex™ KIT Mastocytosis qPCR Assay</tradeName>
    <deviceName></deviceName>
    <manufacturerName>PentaBase A/S</manufacturerName>
    <manufacturerSrn>DK-MF-000023157</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
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    <placedOnMarketCountry>Denmark</placedOnMarketCountry>
    <lastUpdated>2026-06-20T23:33:17.102Z</lastUpdated>
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    <udiDi>05298004820228</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit Aortopathy Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf A</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET203-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:43.069Z</lastUpdated>
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    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Arrhythmia Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf A</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET204-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:43.039Z</lastUpdated>
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    <udiDi>05298004820280</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Cardiomyopathy Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf A</riskClass>
    <legislation>UNKNOWN</legislation>
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    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET205-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:43.007Z</lastUpdated>
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    <udiDi>05298004820310</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Congenital Heart Defects Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET206-00- 2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.986Z</lastUpdated>
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    <udiDi>05298004820341</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - FH, PH and RAS Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf A</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET207-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.962Z</lastUpdated>
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    <udiDi>05298004820372</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Cardiac Comprehensive Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>IVD Sınıf A</riskClass>
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    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET210-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.942Z</lastUpdated>
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    <udiDi>05298004820402</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Hereditary Cancer Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET211-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.913Z</lastUpdated>
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    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Infertility Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
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    <reference>ET212-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.891Z</lastUpdated>
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    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Neonatal Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET213-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.869Z</lastUpdated>
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    <tradeName>TarCET Kit - Carrier Screening Core Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET214-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.852Z</lastUpdated>
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    <tradeName>TarCET Kit - Carrier Screening Comprehensive Panel</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
    <manufacturerSrn>CY-MF-000009381</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>ET215-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.823Z</lastUpdated>
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    <tradeName>BRAF Codon 600 Mutation Analysis Kit II</tradeName>
    <deviceName></deviceName>
    <manufacturerName>EntroGen, Inc.</manufacturerName>
    <manufacturerSrn>US-MF-000022721</manufacturerSrn>
    <authorisedRepresentativeName>TANJA TOPOVSEK S.P.</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>SI-AR-000022518</authorisedRepresentativeSrn>
    <riskClass>IVD Genel</riskClass>
    <legislation>UNKNOWN</legislation>
    <emdnCode>W01060299</emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BRAFX-RT64</reference>
    <placedOnMarketCountry>Slovenia</placedOnMarketCountry>
    <lastUpdated>2026-06-19T21:01:31.515Z</lastUpdated>
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