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

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    MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    K'FIX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORALUBE

    FDA 510(k)
    FDA Class 1 ·Dental

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 8, 2013

    SHILEY DISPOSABLE CANNULA LOW PRESSURE

    FDA Adverse Event
    Injury ·COVIDIEN / FORMERLY TYCO HEALTHCARE·Product code JOH·March 24, 2011

    STERRAD 200 STERILIZATION SYSTEM

    FDA Adverse Event
    Malfunction ·YAMATO LAB-TECH CO., LTD·Product code MLR·May 9, 2008

    VITEK® 2 AST-N350

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 17, 2018

    VITEK® 2 AST-N350

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 17, 2018