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

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    KIMBERLY-CLARK SELF-SEAL POUCH FOR LOW TEMPERATURE STERILIZATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    MYCOLOGY W/CYCLOHEXANIDE & CHLORAMPHEMICOL (C&C)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LightScalpel

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    2520274-2013-10514

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNI·February 19, 2013

    LASSO? ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·August 1, 2014

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·January 14, 2011