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    <tradeName>PlentiPlex™ MYD88 Waldenström Lymphoma qPCR Assay</tradeName>
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    <basicUdiDi>5713915PP001TD</basicUdiDi>
    <tradeName>PlentiPlex™ KIT Mastocytosis qPCR Assay</tradeName>
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    <manufacturerName>PentaBase A/S</manufacturerName>
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    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit Aortopathy Panel</tradeName>
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    <manufacturerName>MEDICOVER GENETICS LIMITED</manufacturerName>
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    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
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    <reference>ET203-00-2016</reference>
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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>
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    <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>
    <emdnCode>W01060299</emdnCode>
    <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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    <legislation>UNKNOWN</legislation>
    <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>
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    <legislation>UNKNOWN</legislation>
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    <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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    <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>
    <legislation>UNKNOWN</legislation>
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    <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>
    <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>ET211-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.913Z</lastUpdated>
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    <udiDi>05298004820433</udiDi>
    <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>
    <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>ET212-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.891Z</lastUpdated>
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    <udiDi>05298004820464</udiDi>
    <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>
    <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>ET213-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.869Z</lastUpdated>
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    <udiDi>05298004820495</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Carrier Screening Core 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>ET214-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.852Z</lastUpdated>
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    <udiDi>05298004820525</udiDi>
    <basicUdiDi>52980048MULTITN</basicUdiDi>
    <tradeName>TarCET Kit - Carrier Screening Comprehensive 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>ET215-00-2016</reference>
    <placedOnMarketCountry>Cyprus</placedOnMarketCountry>
    <lastUpdated>2026-06-20T21:23:42.823Z</lastUpdated>
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    <udiDi>05060536830101</udiDi>
    <basicUdiDi>B-05060536830101</basicUdiDi>
    <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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    <udiDi>04251315811423</udiDi>
    <basicUdiDi>B-04251315811423</basicUdiDi>
    <tradeName>XL PAX5 BA</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></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>D-5143-100-OG</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-17T15:21:08.742Z</lastUpdated>
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    <basicUdiDi>B-04251315811300</basicUdiDi>
    <tradeName>XL 5p15/21q22</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></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>D-5155-100-OG</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-17T15:21:07.899Z</lastUpdated>
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    <basicUdiDi>B-04251315811294</basicUdiDi>
    <tradeName>XL CUX1/EZH2/7cen</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></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>D-5144-100-TC</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-17T15:21:06.950Z</lastUpdated>
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    <basicUdiDi>B-04251315811058</basicUdiDi>
    <tradeName>XL t(4;11) AFF1/KMT2A DF</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></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>D-5131-100-OG</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-17T15:21:06.093Z</lastUpdated>
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    <udiDi>04251315810976</udiDi>
    <basicUdiDi>B-04251315810976</basicUdiDi>
    <tradeName>XL ABL1 BA</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></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>D-5148-100-OG</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-17T15:20:59.045Z</lastUpdated>
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    <udiDi>04251315810679</udiDi>
    <basicUdiDi>B-04251315810679</basicUdiDi>
    <tradeName>XL CSF1R BA</tradeName>
    <deviceName></deviceName>
    <manufacturerName>MetaSystems Probes GmbH</manufacturerName>
    <manufacturerSrn>DE-MF-000006315</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></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>D-5152-100-OG</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-17T15:20:57.229Z</lastUpdated>
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