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

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    OREGON FIXATION SYSTEM INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OEC 9800 PLUS

    FDA 510(k)
    FDA Class 2 ·Radiology

    CHOLESTECH LDX ASPARTATE AMINOTRANSFERASE (AST)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    UNKNOWN SALINE IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·July 21, 2020

    JUVEDERM ULTRA PLUS XC TSK US

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·June 20, 2014

    ITREL 3

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·November 30, 2010

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·January 28, 2013

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·July 20, 2020

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·December 7, 2018