BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NUVASIVE

    FDA Adverse Event
    Injury ·NUVASIVE·Product code NKB·January 10, 2011

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 16, 2007

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 12, 2013

    HEARTSTRING III PROXIMAL SEAL SYSTEM, 3.8 MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·February 1, 2011

    PREMICRON GREEN 4/0(1,5)4X45 HR13 TOM

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·January 29, 2020

    PREMICRON GREEN 2/0 (3) 75CM HR26 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAW·June 28, 2019

    ANTI-HUMAN GLOBULIN ANTI-IGG (RABBIT) (GREEN) IH-CARD AHG ANTI-IGG

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHS·September 3, 2020

    PREMICRON GREEN 2/0 (3) 30CM SKR19(M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·February 3, 2020

    PREMICRON G/W 2/0(3)4X90CM2XHRC20MPF6MLP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·December 30, 2019

    PREMICRON GREEN 2/0 (3) 75CM HR26 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·December 30, 2019

    PREMICRON G/W 2/0(3)4X90CM2XHRC20MPF6MLP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·December 30, 2019