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

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    SERUM IRON/VIBC REAGENT SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209118175·

    POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Thoratec CentriMag Return (Arterial) Cannula Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2A-TAPER LINER SZ 41/32

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 5, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCO·Product code CBK·November 12, 2012

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 29, 2010