BEUDAMED
    37 results · 29ms · Sources: EU EUDAMED, US FDA

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    BICON TRANSITIONAL IMPLANT (BTI) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00811801036262·Reusable Jamshidi - Bevel Stylet

    SunMed

    FDA UDI
    SUNMED, LLC·10889483041277·CONV C/P EXTRA LARGE HANDLE D

    ACT III VENTRICULAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    XTRAC EXCIMER LASER SYSTEM, MODEL AL7000

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NONE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 3, 2008

    SYNCHRO 14 NEURO GUIDEWIRE

    FDA Adverse Event
    Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007

    SYNCHRO -10 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006

    SYNCHRO-14 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006

    SYNCHRO 14 GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

    SYNCHRO .014 GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007

    SYNCHRO .014 GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007

    SYNCHRO -14 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code DQX·November 30, 2006

    SYNCHRO-14 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQX·September 12, 2007

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

    STERRAD 100NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·March 27, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·February 24, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·August 15, 2014

    SYNCHRO 14 "S" NEURO GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

    SYNCHRO 10 NEURO GUIDEWIRE

    FDA Adverse Event
    Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DQX·November 7, 2007