BEUDAMED
    6 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    0009613348-2024-014247

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·October 23, 2024

    DIALYSIS UNKNOWN

    FDA Adverse Event
    Injury ·COVIDIEN MFG SOLUTIONS S.A.·Product code FJS·April 22, 2019

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·December 17, 1997

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 6, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 10, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·March 12, 2008