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

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    Filters FDA Adverse Event ×

    VANG DIST FEM AUG 65X5 RL/LM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 20, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 26, 2011

    4 MOTOR ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·March 14, 2016