BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    Powerheart G5 AED

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    POWERHEART G5 AUTOMATIC AED

    FDA Adverse Event
    Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·October 18, 2018

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550193·GENUMEDI PT KNEE SUP SILVER R EW IV

    OSSIX BONE, OSSIX PLUS

    FDA Adverse Event
    Injury ·DATUM DENTAL LTD.·Product code NPM·June 22, 2022

    PRECISION MONTAGE MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 14, 2020

    ENCORE ACCLAIM STERILE POWDER-FREE LATEX SURGICAL GLOVES, TESTED FOR USE WITH CHEMOTHERA

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    VPAP TX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 3, 2013

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·June 3, 2011

    CENTRICITY RA1000

    FDA Adverse Event
    Injury ·GE HEALTHCARE INTEGRATED IT SOLUTIONS·Product code LLZ·August 29, 2008