BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    COMPREHENSIVE PHOROPTER, MDR-680

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    MONOSTERYL

    FDA 510(k)
    FDA Class 1 ·Dental

    ELECTRIC WIRE DRIVER, MODEL 2640E

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 30, 2013

    ARROW BLUEGARD

    FDA Adverse Event
    ARROW INTERNATIONAL·Product code DQY·December 9, 2010

    ARCHITECT PHOSPHORUS

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 15, 2014