BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    OSTEONICS SCORPIO TOTAL KNEE UNIVERSAL DOME PATELLAR COMPONENT;OSTEONICS SCORPIO TOTAL KNEE RECESSED PATELLAR COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CANNULATED CRUCIFORM SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·October 25, 2016

    QUANTA LITE F-ACTIN IGA ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    Mercury® Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016

    PORTEX® BIVONA® AIRE-CUF® ADULT TRACHEOSTOMY TUBES

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD INC.·Product code JOH·September 1, 2016

    HERMETIC II EXTERNAL CSF DRAINAGE MGMT

    FDA Adverse Event
    Malfunction ·HEYER-SCHULTE NEUROCARE, INC.·Product code JXG·March 19, 1998

    PINN CAN BONE SCREW 6.5MMX25MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code HWC·February 21, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·January 20, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·August 1, 2014

    CANNULATED CRUCIFORM SCREWDRIVER

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HXX·May 5, 2020