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    <emdnDescription></emdnDescription>
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    <tradeName>CA CLEAN II</tradeName>
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    <emdnDescription></emdnDescription>
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    <deviceName></deviceName>
    <manufacturerName>SYSMEX CORPORATION</manufacturerName>
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    <emdnDescription></emdnDescription>
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    <manufacturerName>SYSMEX CORPORATION</manufacturerName>
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    <emdnDescription></emdnDescription>
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    <manufacturerName>SYSMEX CORPORATION</manufacturerName>
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    <emdnDescription></emdnDescription>
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    <deviceName></deviceName>
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    <tradeName>Prenatal 13 and 21 Enumeration Probe kit</tradeName>
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    <manufacturerName>Cytocell Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000016893</manufacturerSrn>
    <authorisedRepresentativeName>Sysmex Europe SE</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000022333</authorisedRepresentativeSrn>
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    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>DOWN'S SYNDROME</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CE-LPA 003-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-27T18:20:56.975Z</lastUpdated>
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    <tradeName>BCR/ABL (ABL1) Translocation, Dual Fusion Probe</tradeName>
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    <manufacturerName>Cytocell Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000016893</manufacturerSrn>
    <authorisedRepresentativeName>Sysmex Europe SE</authorisedRepresentativeName>
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    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>T (9;22)</emdnDescription>
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    <reference>CE-LPH 007-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-27T18:20:56.932Z</lastUpdated>
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    <tradeName>ATM Deletion Probe</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Cytocell Limited</manufacturerName>
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    <authorisedRepresentativeName>Sysmex Europe SE</authorisedRepresentativeName>
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    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CE-LPH 011-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-27T18:20:56.890Z</lastUpdated>
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    <tradeName>MLL (KMT2A) Breakapart Probe</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Cytocell Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000016893</manufacturerSrn>
    <authorisedRepresentativeName>Sysmex Europe SE</authorisedRepresentativeName>
    <authorisedRepresentativeSrn>DE-AR-000022333</authorisedRepresentativeSrn>
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    <emdnCode></emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CE-LPH 013-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-27T18:20:56.855Z</lastUpdated>
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    <tradeName>Del(20q) Deletion Probe</tradeName>
    <deviceName></deviceName>
    <manufacturerName>Cytocell Limited</manufacturerName>
    <manufacturerSrn>GB-MF-000016893</manufacturerSrn>
    <authorisedRepresentativeName>Sysmex Europe SE</authorisedRepresentativeName>
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    <emdnCode></emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
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    <reference>CE-LPH 020-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
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    <emdnCode></emdnCode>
    <emdnDescription>INV (16)</emdnDescription>
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    <reference>CE-LPH 022-S</reference>
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    <reference>CE-LPH 024-S</reference>
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    <reference>CE-LPH 025-S</reference>
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    <manufacturerName>Cytocell Limited</manufacturerName>
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    <reference>CE-LPH 026-S</reference>
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    <lastUpdated>2026-06-27T18:20:56.665Z</lastUpdated>
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    <emdnCode></emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CE-LPH 027-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-27T18:20:56.624Z</lastUpdated>
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    <legislation>UNKNOWN</legislation>
    <emdnCode></emdnCode>
    <emdnDescription>TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>CE-LPH 036-S</reference>
    <placedOnMarketCountry>Germany</placedOnMarketCountry>
    <lastUpdated>2026-06-27T18:20:56.578Z</lastUpdated>
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