BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event × Status: No Answer Provided × Clear all

    NEOLEAD RADIOLUCENT

    FDA Adverse Event
    No answer provided ·NEOTECH PRODUCTS LLC·Product code DRX·March 17, 2023

    ARROW

    FDA Adverse Event
    No answer provided ·ARROW INTERNATIONAL, LLC·Product code MPB·March 15, 2023

    BILATERAL KNEE PACK

    FDA Adverse Event
    No answer provided ·CARDINAL HEALTH 200, LLC·Product code OJH·March 14, 2023

    MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

    FDA Adverse Event
    No answer provided ·PHILIPS NORTH AMERICA LLC·Product code MHX·February 14, 2023

    INSTRUMENT, ULTRASONIC SURGICAL

    FDA Adverse Event
    No answer provided ·ETHICON ENDO-SURGERY, LLC·Product code LFL·February 7, 2023

    CARDINAL HEALTH

    FDA Adverse Event
    No answer provided ·CARDINAL HEALTH 200, LLC·Product code LRO·November 14, 2022

    FORMALIN

    FDA Adverse Event
    No answer provided ·SLMP LLC (STATLAB MEDICAL PRODUCTS)·Product code IFP·April 13, 2022