BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    OMNI-FIX, HUMERAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PicoWay Laser System CPO

    FDA UDI
    Candela Corporation·00817495022819·PicoWay Laser System CPO

    CD 3700 SL

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

    PILLCAM PLATFORM WITH PILLCAM SB CAPSULES WITH PILLCAM SENSORBELT

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

    125I LEUTINIZING HORMONE RIA KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    WHITE RELOAD FOR ECHELON

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 6, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·January 27, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014