BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    MONODEX

    FDA 510(k)
    FDA Class 2 ·Immunology

    SUPRIMA 253-21 IMPLANTABLE PULSE GENERATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MONOPOLAR INJECTION NEEDLE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 25, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·November 5, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·December 20, 2012