BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    IN-LINE HEMOSTASIS VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEROYAL NON-LOCKING BONE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Plexus SCD110 Sequential Compression Device Sleeve

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    32MM I.D. SIZE LL ELEVATED RIM LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 4, 2022

    COBAS B 123 <4> SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CHL·March 6, 2013

    SHILEY DISPOSABLE CANNULA FENESTRATED

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code JOH·February 10, 2011

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014