BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    COLISCREEN

    FDA 510(k)
    FDA Class 1 ·Microbiology

    C-STEM

    FDA UDI
    DEPUY INTERNATIONAL LTD·10603295235484·C-STEM BROACH SIZE 1

    FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Latera Absorbable Nasal Implant

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 28, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 18, 2013

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·January 11, 2011

    20MM COCR RADIAL HEAD 4MM HT EXTENSION/16.0MM-STER

    FDA Adverse Event
    Injury ·SYNTHES USA PRODUCTS LLC·Product code KWI·January 19, 2018

    FT3 - FREE TRIIODOTHYRONINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·October 10, 2014

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·September 30, 2016