BEUDAMED
    1,792 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 15, 2024

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 11, 2019

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 11, 2019

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·May 18, 2022

    SEQUOIA FINAL DRIVER (PLE)

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·April 25, 2012

    SEQUOIA FINAL DRIVER (PLE)

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 8, 2011

    SEQUOIA FINAL DRIVER (PLE)

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 8, 2011

    SEQUOIA FINAL DRIVER (PLE)

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·March 25, 2011

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PLE. LTD.·Product code FRN·March 28, 2003

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQM·June 30, 2017

    META DDDR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2006

    ETHICON

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY LLC·Product code PLE·April 3, 2017

    SUPERDIMENSION INREACH SYSTEM

    FDA Adverse Event
    Malfunction ·SUPERDIMENSION INC.·Product code JAK·March 30, 2011

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·January 18, 2017

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·January 20, 2017

    VITEK® 2 GN ID CARD

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·December 28, 2016

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 22, 2023

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·November 14, 2012

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LQM·November 22, 2017

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LQM·November 22, 2017