BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    NEXUS

    FDA 510(k)
    FDA Class 2 ·Dental

    MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEPANORM CALIBRATION PLASMA SET

    FDA 510(k)
    FDA Class 2 ·Hematology

    HENRY SCHEIN

    FDA Adverse Event
    Injury ·AMD MEDICOM·Product code FXX·May 1, 2026

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·February 11, 2013

    PROMOTE RF CRT-D

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

    TIGERPAW SYSTEM II

    FDA Adverse Event
    Injury ·LAAX INC.·Product code GDW·July 18, 2014

    Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017