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

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    Filters Regulation: Us FDA ×

    SYNCHRON SYSTEMS CANNABINOID 20 NG REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    JEJUNO-CATH KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    AUTOCHILL ACCESSORY KIT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·June 11, 2014

    UNIVERSAL STEM 75X12MM FLUTED

    FDA Adverse Event
    Injury ·DEPUY RAYNHAM·Product code JWH·February 11, 2013

    TENDRIL ST

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

    VIDAS ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·January 21, 2021

    VIDAS® ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·September 16, 2021

    Bivona Aire-Cuf Endotracheal Tube

    FDA Enforcement
    Class II ·Terminated·Smiths Medical ASD Inc.·November 3, 2021