BEUDAMED
    32 results · 28ms · Sources: EU EUDAMED, US FDA

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    TRINITY POLYAXIAL SCREW, MEHDIAN SPINAL ROD (6MM), MODEL 159.XXX SERIES CATALOGUE NUMBERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890107760·Zirlux UCLA Plastic Abut N Eng

    General Instruments

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746162428·INSTRUMENT MATHIEU NEEDLE HOLDER SUPER FINE TI...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450329375·

    SCREW, FIXATION, BONE

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

    MEDTRONIC DLP ARTERIAL CANNULAE WITH 3D TIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO HP M2376A DEVICE LINK SYSTEM, MODEL M2376A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STEM: M-VIZION DISTAL STEM Ø14MM L 180MM STRAIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 9, 2023

    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

    GENESYS HTA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code MNB·March 13, 2013

    UNKNOWN SOFRADIM PRODUCT

    FDA Adverse Event
    Malfunction ·SOFRADIM PRODUCTION·Product code FTL·January 6, 2010

    ATLAS + VR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·March 10, 2008

    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

    DANTEC CONCENTRIC NEEDLES

    FDA Adverse Event
    Malfunction ·NATUS MANUFACTURING LIMITED·Product code IKT·April 22, 2022