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

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    Filters FDA Adverse Event ×

    LEVIN TUBE

    FDA Adverse Event
    Death ·DAVOL INC. SUBSIDIARY OF CR BARD INC.·Product code FPD·March 24, 1997

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS - HOUSTON·Product code MUZ·November 10, 2017

    ENDOPATH ELECTROSURGERY PROBE PLUS II

    FDA Adverse Event
    Malfunction ·EES-JUAREZ·Product code KNS·February 19, 1997

    ENDOPATH THORACIC ENDOLINEAR CUTTER W/SAFETY LOCKOUT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·January 30, 1997

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 21, 2013

    1X8 SUB COMPACT TEST STIMULATION LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code GZB·January 6, 2011

    UNK M/L TAPER STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LZO·July 8, 2014

    ENDOPATH TRISTAR EXTRAPERITONEAL DISSECTOR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·May 8, 1997