BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    CARDIO-WRAP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD PRECISIONGLIDE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·August 1, 2023

    CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SONOTOME ULTRASONIC ASPIRATOR TIPS

    FDA 510(k)
    FDA Unclassified ·Unknown

    BD PRECISIONGLIDE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·August 1, 2023

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 2, 2013

    ETRIO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·September 15, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 19, 2011