BEUDAMED
    1,046 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    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

    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

    VITEK® 2 GRAM NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQM·October 18, 2018

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·December 30, 2016

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LQM·August 28, 2017

    STAPLE, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 10, 2013

    STAPLE, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 10, 2013