BEUDAMED
    Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

    RapidFor™ CA 15-3 Rapid Test Kit (FIA)

    Vitrosens Biyoteknoloji Anonim Şirketi · 🇹🇷 Türkiye
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    Devices (same UDI-DI)
    1
    Certificates
    0
    Countries
    0
    Notified Bodies
    0

    Basic Information

    Primary DI
    08684595030219
    Basic UDI-DI Code
    B-08684595030219
    Reference
    VMPO84
    Device Types
    Single use
    Regulation
    Eu Ivdd
    Classification
    Eu Ivd General
    Status
    On The Market
    Manufacturer
    Vitrosens Biyoteknoloji Anonim Şirketi

    Additional Description

    The CA 15-3 Rapid Test Kit (FIA) is intended for the qualitative detection of CA 15-3 antigen in human serum or plasma samples.

    CND Nomenclature Codes

    Code Description
    W0102030102 CANCER ANTIGEN 15-3

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