BEUDAMED
    5 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SMR GLENOID BASEPLATE STANDARD

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWS·April 18, 2019

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 23, 2012

    MAGIC 3 FEMALE INTERMITTENT CATHETER

    FDA Adverse Event
    Malfunction ·ROCHESTER MEDICAL CORP·Product code KOD·May 27, 2015

    BREATH RIGHT ORIGINAL

    FDA Adverse Event
    Injury ·WEBTEC DIV OF SCARPA HEALTHCARE·Product code LWF·May 20, 2019