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

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    ProxiFuse Hammer Toe Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IGX PLEX CELIAC QUALITATIVE ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    ELECSYS FOLATE II CALSET II

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 2/11 MM LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 23, 2017

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 6, 2014

    EVOLUTION COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MQR·May 8, 2013

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 28, 2011