BEUDAMED
    Eu Ivdr Eu Ivd Class B On The Market ๐Ÿ‡จ๐Ÿ‡ฟ Czechia

    AMH Gen II ELISA

    IMMUNOTECH s.r.o. ยท ๐Ÿ‡จ๐Ÿ‡ฟ Czechia
    View on EUDAMED
    Devices (same UDI-DI)
    1
    Certificates
    0
    Countries
    25
    Notified Bodies
    0

    Basic Information

    Primary DI
    15099590206703
    Basic UDI-DI Code
    150995905A79765VK
    Reference
    A79765
    Device Types
    None provided
    Regulation
    Eu Ivdr
    Classification
    Eu Ivd Class B
    Status
    On The Market
    Manufacturer
    IMMUNOTECH s.r.o.

    Additional Description

    AMH Gen II ELISA is an in vitro diagnostic manual medical device intended to be used by healthcare professionals for the quantitative measurement of Anti-Mรผllerian hormone (AMH) in human serum and plasma. Measurement of AMH is intended to be used for the assessment of fertility status and sexual development. In females, it is used to assess ovarian and menopausal status, including ovarian reserve, and as an aid in diagnosis of PCOS. It is used as an aid in differential diagnosis of intersex conditions in infants.

    CND Nomenclature Codes

    Code Description
    W0102050215 ANTI-Mร›LLERIAN HORMONE

    Available In Countries

    ๐Ÿ‡ฆ๐Ÿ‡น Austria ๐Ÿ‡ง๐Ÿ‡ช Belgium ๐Ÿ‡ง๐Ÿ‡ฌ Bulgaria ๐Ÿ‡จ๐Ÿ‡พ Cyprus ๐Ÿ‡จ๐Ÿ‡ฟ Czechia ๐Ÿ‡ฉ๐Ÿ‡ช Germany ๐Ÿ‡ฉ๐Ÿ‡ฐ Denmark ๐Ÿ‡ฌ๐Ÿ‡ท Greece ๐Ÿ‡ช๐Ÿ‡ธ Spain ๐Ÿ‡ซ๐Ÿ‡ฎ Finland ๐Ÿ‡ซ๐Ÿ‡ท France ๐Ÿ‡ญ๐Ÿ‡บ Hungary ๐Ÿ‡ฎ๐Ÿ‡ช Ireland ๐Ÿ‡ฎ๐Ÿ‡น Italy ๐Ÿ‡ฑ๐Ÿ‡ฎ Liechtenstein ๐Ÿ‡ฑ๐Ÿ‡น Lithuania ๐Ÿ‡ฑ๐Ÿ‡บ Luxembourg ๐Ÿ‡ฒ๐Ÿ‡น Malta ๐Ÿ‡ณ๐Ÿ‡ฑ Netherlands ๐Ÿ‡ณ๐Ÿ‡ด Norway ๐Ÿ‡ต๐Ÿ‡ฑ Poland ๐Ÿ‡ต๐Ÿ‡น Portugal ๐Ÿ‡ธ๐Ÿ‡ช Sweden ๐Ÿ‡ธ๐Ÿ‡ฐ Slovakia ๐Ÿ‡น๐Ÿ‡ท Tรผrkiye

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