BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    HARBORIN CENTRAL VENOUS CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    V. MUELLER PHEUMO-INTESTINAL INSTRUMENT SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CHURCHILL-HCM VENTED IV SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    130 DEG AIMING ARM F/TROCHANTERIC FIXATION NAILS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·May 24, 2013

    BUTTRESS/COMPRESSION NUT FOR 357.369

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code HST·May 24, 2013

    EASYTRAK 2

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NIK·July 1, 2015

    ULTRASONIC IMAGING CATHETER - CORONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·June 19, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 22, 2010

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020