BEUDAMED
    11 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IV SET AN120 W/O BP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code LHI·February 20, 2019

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    TRANSVENE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 31, 2012

    NIM EMG ENDOTRACHEAL TUBE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code BTR·August 18, 2010

    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

    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

    IV SET AN120 W/O BP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FRN·April 1, 2019