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

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    SLEEPSCAN AIRFLOW PRESSURE TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ICU Medical

    FDA UDI
    ICU MEDICAL, INC.·00887709044500·7" (18 cm) Appx 0.42 ml, Pressure Infusion (400...

    ANEROID SPHYGMOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE

    FDA 510(k)
    FDA Not Classified ·Unknown

    SYNCHRON® ALT REAGENT, 2 X 200 TEST

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·July 26, 2011

    VIVACIT-E DM LINER 28 X 38MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 25, 2020

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2013

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·January 21, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 31, 2014

    VIVACIT-E DM LINER 28 X 38MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 8, 2020