BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    GR Resin System MSI

    FDA 510(k)
    FDA Unclassified ·Unknown

    UNIVERSAL NEURO 3 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    PRECISET DAT PLUS I CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MX40 1.4 GHZ SMART HOPPING

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DSI·October 14, 2014

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 1, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 17, 2013

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022