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

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    MIRI TL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111451768·BUCK SUTURE SCISS STR 5.75 INCHES

    DS7A CONSTANT CURRENT HIGH VOLTAGE STIMULATOR, MODEL DS7A; DS7AH CONSTANT CURRENT HIGH VOLTAGE STIMULATOR, MODEL DS7AH

    FDA 510(k)
    FDA Class 2 ·Neurology

    STRAUMANN NARROW NECK CROSSFIT (NNC) 03.3MM DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ONE TOUCH BASIC ENHANCED

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 20, 2002

    ONE TOUCH BASIC ENHANCED

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 23, 2002

    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

    ROSA ONE

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

    ROSA ONE

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

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 30, 2013

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

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

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 6, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 3, 2018