BEUDAMED
    6 results · 43ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 7, 2024

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 7, 2024

    HEARTMATE II LVAS, EUROPE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 27, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·January 30, 2013

    COOL PATH 7F, 1304-CP-7-25-L-AB (USA)

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL, IRVINE·Product code OAD·November 24, 2010

    SHELL POROUS WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·May 26, 2017