BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Cortex Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    SECURVIEW DX DIAGNOSTIC WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    DUREX PLAY MASSAGE GEL LUBRICANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DEPTH ELECTRODE

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·December 14, 2021

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    ASR 300 SPIKED CUP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 8, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·September 10, 2008

    HEARTMATE II LEFT VENTRICULAR ASSIST SYSTEM, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·October 26, 2018