BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ICU MEDICAL PRIMARY PLUM SET ORANGE PE LINED

    FDA Adverse Event
    Injury ·ICU MEDICAL, INC.·Product code FPA·December 13, 2022

    PERF CON TIB BRG XSML 22X60

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·March 23, 2018

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    PRIMARY PLUM SET, ORANGE POLYETHYLENE LINED LIGHT RESISTANT TUBING, CLAVE Y-SITE

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·November 11, 2022

    CUSTOM PAK

    FDA Adverse Event
    Injury ·ALCON - HOUSTON·Product code KYG·June 27, 2014

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 7, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 3, 2010