BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    X3 Exp/X3/X3 Pro/X1 Pro/X1 Digital Color Doppler Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM

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

    MOBILEECG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·July 28, 2017

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·July 28, 2017

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 11, 2013

    MAXI MOVE

    FDA Adverse Event
    Injury ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·July 4, 2011

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·August 10, 2008