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

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    VITA-STAT MODEL 9000-A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT)

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDLINE VESSEL CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 24, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·August 13, 2010

    BD DISCARDIT II 2 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 10, 2019

    BD DISCARDIT II 2 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 6, 2019