BEUDAMED
    2,001 results · 29ms · Sources: EU EUDAMED, US FDA

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    Frontier Electric Wheelchair

    FDA UDI
    RED MILAWA PTY. LTD.·09356399000017·Frontier V4 Front Wheel Drive Electric Wheelchair

    Hoveround

    FDA UDI
    HOVEROUND CORPORATION·00859781000026·Wheelchair, powered

    ARROW FWD POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    QUICKIE INTERCHANGE FWD W/LIFT POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Frontier V4

    FDA UDI
    SUNRISE MEDICAL (US) LLC·00016958059717·The Magic Mobility Frontier V4 Front-Wheel Driv...

    BATTERY REAMER/DRILL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·July 30, 2016

    GALILEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·October 13, 2011

    ORTHO VISION ID-MTS ANALYZER

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·August 3, 2022

    KERRISON RONGEUR(40° FWD)4MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code HTX·September 23, 2016

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWB·November 26, 2014

    COLIBRI II HANDPIECE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·December 19, 2023

    GALILEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·March 3, 2008

    GALILEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·October 22, 2008

    GALILEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·December 7, 2006

    GAAB OP SCOPE STR FWD 0

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code GWG·April 3, 2000

    KERRISON RONGEUR (40 DEG FWD), 4MM

    FDA Adverse Event
    Malfunction ·ABBOTT SPINE·Product code HTX·October 7, 2008

    KERRISON RONGEUR (40 DEG FWD), 4MM

    FDA Adverse Event
    Injury ·ZIMMER SPINE·Product code HTX·December 8, 2009

    KERRISON RONGEUR (40 DEG FWD), 4MM

    FDA Adverse Event
    Malfunction ·ABBOTT SPINE·Product code HTX·June 26, 2008

    KERRISON RONGEUR (40 DEG FWD), 2MM

    FDA Adverse Event
    Injury ·ABBOTT SPINE·Product code HTX·May 14, 2008