BEUDAMED
    67 results · 24ms · Sources: EU EUDAMED, US FDA

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    COULTER® LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·December 3, 2012

    RECON SAGITTAL SAW WITH KEY FOR TRAUMA RECON SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code GEY·June 6, 2014

    CORDLESS DRIVER 2 HANDPIECE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HRX·September 7, 2010

    UNKNOWN COONRAD-MORREY ULNAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY ULNAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY POLYETHYLENE BUSHING

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 14, 2017

    UNKNOWN COONRAD-MORREY ULNAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 15, 2017

    EXPLOR 7X26MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·April 25, 2017

    EXPLOR 7X26MM IMPLANT STEM WITH SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·April 24, 2017

    EXPLOR 8X28MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·April 25, 2017

    EXPLOR 7X26 MM IMPLANT STEM WITH SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·May 2, 2017