BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Carto Octaray Mapping Catheter with Trueref Technology

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LANX SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERTUS 140 2.45GHZ ABLATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·July 13, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·June 27, 2013

    POWER DRIVE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·October 22, 2014

    GLENOSPHERE 38MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·February 3, 2023

    TRUE METRIX

    FDA Adverse Event
    Injury ·TRIVIDIA HEALTH INC·Product code NBW·September 7, 2023