BEUDAMED
    5 results · 20ms · 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 FDA Adverse Event ×

    GRAFTON DBM

    FDA Adverse Event
    Injury ·MEDTRONIC EATONTOWN·Product code NUN·July 6, 2019

    TI COLLAR WITH GROOVES

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code MNI·April 22, 2013

    CIDEX ACTIVATED DIALDEHYDE SOLUTION

    FDA Adverse Event
    Injury ·ADVANCED STERILIZATION PRODUCTS·Product code LRJ·April 27, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 10, 2008

    BD TEXIUM¿ NEEDLE-FREE SYRINGE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FMF·November 29, 2022