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

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    BLAZER™ Dx-20 Bidirectional Steerable Diagnostic Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    232651

    FDA Adverse Event
    Death ·June 30, 1999

    NOA Sleep Apnea and Snoring Device

    FDA 510(k)
    FDA Class 2 ·Dental

    ITCLAMP 50

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 12, 2024

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·August 18, 2011

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·September 12, 2014

    16" VAC STERILIZER

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·July 18, 2013