BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    UROTRACT I

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837194352·

    DURAHESIVE PROTECTIVE BARRIER WIPE

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    INFINITY 252

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024157811·

    5.5X20MM PERIPHERAL SCREW, LOCKING

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·May 20, 2020

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    ENDURON 10D 60 OR 72ODX28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 11, 2013

    UNKNOWN

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·July 24, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011