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

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    Filters FDA Adverse Event ×

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

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    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    CERELINK ICP PROBE BASIC KIT

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code GWM·August 22, 2023

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    INNOVA 3100-IQ

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS SCS·Product code OWB·March 21, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVY·October 31, 2012

    1644487-2008-00522

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008