BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    IMPREGUM F

    FDA 510(k)
    FDA Class 2 ·Dental

    APEX HP M ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODEL 8800 BIPOLAR COAGULATION THERAPEUTIC SYSTEM

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

    NOTINGHM SHLDR HUM HEAD 48X17 OFFSET

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·January 19, 2016

    DIDECO COMPACTFLO EVOLUTION OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 15, 2016

    CATALYS PRECISION LASER SYSTEM

    FDA Adverse Event
    Injury ·OPTIMEDICA CORPORATION·Product code OOE·March 2, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·February 4, 2011

    PROTECTA XT CRT-D

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code NIK·August 8, 2014