BEUDAMED
    43 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    CONCORDE Bullet Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OXIMAX NPB-40 HANDHELD PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TALON DISTALFIX PROXIMAL FEMORAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·April 11, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 15, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·June 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 16, 2017

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code CBK·June 20, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2017

    32MM COCR MOD HD +6MM NO SKIRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 2, 2018

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code CBK·August 1, 2017

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·July 25, 2017

    32MM MOD HEAD COCR STD NECK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 25, 2018

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·August 17, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·January 26, 2018

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 8, 2014

    NEXGEN LPS PROVISIOAL ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·June 21, 2011