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

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    Filters FDA Adverse Event ×

    K012364

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 3, 2015

    DELTA CER HEAD 11/13 32MM +6

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LZO·August 5, 2014

    DELTA CER INSERT 36ID X 62OD

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code MRA·August 5, 2014

    DELTA CER HEAD 11/13 36MM +9

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LZO·August 5, 2014

    MONOPOLAR CAUTERY INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 15, 2014

    IMPLANTABLE PACING LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, B.V.·Product code DTB·October 31, 2012

    SUPER POLI-GRIP

    FDA Adverse Event
    Injury ·Product code KOL·August 18, 2010