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

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    Ponto 3, Ponto 3 Power and Ponto 3 SuperPower

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SINGLE SITE FLEXIBLE BLADELESS OBTURATOR

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

    SYNGO TRUED, MODEL VC10A

    FDA 510(k)
    FDA Class 2 ·Radiology

    MECTALIF TRANSFORAMINAL INTERBODY FUSION DEVICE 12X30X8 L°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·September 14, 2018

    CORDLESS GAMMA PROBE COVER

    FDA Adverse Event
    Malfunction ·MICROTEK DOMINICANA, S.A.·Product code KKX·August 18, 2017

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 3, 2013

    JOURNEY GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·July 14, 2011

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·September 15, 2008