BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    FORCEPS CEV405 FENESTRATED 350MM JOHANN [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GEI·March 19, 2014

    UNKNOWN DEPUY SZ. 14X09 S-ROM STEM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code KWA·June 25, 2014

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 2, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·November 4, 2010