BEUDAMED
    8 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

    THERMACHOICE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MKN·June 16, 2006

    THERMACHOICE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MKN·June 16, 2006

    THERMACHOICE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MKN·June 16, 2006

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·February 20, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·January 14, 2011

    6.5CM ADULT CRANI ATTACHMT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 11, 2013

    IMMULITE® 2000 PSA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code MTF·April 26, 2023