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

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    K-ASSAY RHEUMATOID FACTOR CALIBRATOR SET

    FDA 510(k)
    FDA Class 2 ·Immunology

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code OJH·August 31, 2023

    Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V4.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    BABY QUASAR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·March 6, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·February 15, 2011

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014