BEUDAMED
    11 results · 39ms · Sources: EU EUDAMED, US FDA

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    ATTUNE RP TIB BASE SZ 8 CEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code NJL·August 15, 2024

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·April 16, 2013

    KAIROS DR

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO.·Product code DXY·June 13, 2008

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 11, 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

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·August 29, 2018

    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