BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PRECEDENT REVISION HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HeRO Graft

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIVO

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMUFLEX DISPOSBLES

    FDA Adverse Event
    Malfunction ·TERUMO BCT·Product code KSR·February 21, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 1, 2014

    E360 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·January 19, 2011