BEUDAMED
    4,832 results · 44ms · Sources: EU EUDAMED, US FDA

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    Monoart

    FDA UDI
    EURONDA SPA·E30729017413·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017716·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017312·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902041·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017211·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017514·Practical kit Monoart containing 4 different di...

    ASEPT

    FDA UDI
    PFM MEDICAL INCORPORATED·00813623017054·ASEPT Drainage Line Set

    Monoart

    FDA UDI
    EURONDA SPA·E3072902061·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017110·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902101·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729020710·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017817·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902011·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072903501·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902051·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729020811·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902031·Practical kit Monoart containing 5 different di...

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Peripheral Drug- Eluting Stent

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AND VENTAK. MINI AUTOMATIC IMPLANTABLE CARDIOVERTER

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR