BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    HI-TORQUE STEELCORE 18 GUIDE WIRE MODEL NUMBERS 1003280, 1003281, 1003282

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Uro-N Cystoscope

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

    BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY

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

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·January 20, 2025

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 9, 2022

    CRIT-LINE BLOOD CHAMBER

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KOC·June 25, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 31, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·February 9, 2011