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

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    Filters FDA Adverse Event ×

    M2A-MAGNUM PF CUP 48ODX42ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 6, 2022

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 23, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FRN·November 2, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010

    M2A-MAGNUM 42-50MM TPR INSRT-3

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 7, 2019

    MLRY-HD POR FMRL 11X160MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 13, 2018