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

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    KLEENSPEC SINGLE USE VAGINAL SPECULUM AND 790 SERIES CORDLESS ILLUMINATION SYSTEM

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

    STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AUTO-DRIVE LAG SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 11, 2017

    FATHOM GUIDEWIRE

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - FREMONT·Product code DQX·June 16, 2011

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015

    OLYMPUS THUNDERBEAT 5MM, 35CM, PISTOL GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEM CORP·Product code GEI·April 2, 2013

    MIDMARK

    FDA Adverse Event
    Injury ·MIDMARK CORP.·Product code EAZ·April 20, 2011

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·July 3, 2008

    FATHOM GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·February 23, 2010

    FATHOM GUIDEWIRE

    FDA Adverse Event
    Injury ·SALT LAKE CITY·Product code DQX·February 23, 2010