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

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    DTI-1 SLA IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528103050·7.0 x 75mm Cann Hdless Screw, 32mm Thd

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528107416·7.0 x 75mm Hdls Screw 32Thd Sterile 2Pk

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 18, 2015

    SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUPRA OPHTHALMIC LASER PHOTOCOAGULATOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 3, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 4, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 8, 2015

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 14, 2013

    FLEXOR BALKIN GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·September 17, 2008

    GEM PREMIER 4000

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code CHL·June 22, 2011

    VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    VA LOCKSCR Ø2.4 SELF-TAP L24 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    2.4MM TI VA LOCKING SCREW STARDRIVE 22MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 9, 2013

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 11MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·December 22, 2014

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 7, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·October 3, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 10, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 12, 2016