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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    CARDIAC OUTPUR/SATURATED VENOUS OXYGEN MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PAREMA K BAND NON-STERILE

    FDA 510(k)
    FDA Unclassified ·Unknown

    ROCHE ORAL FLUID OPIATES, DAT QUAL CAL A, DAT CONTROL SET A AND DAT SQ CAL A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·June 25, 2014

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code MKJ·November 1, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 2, 2013