BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    CARDIOVISION SOFTWARE, MODEL S-CV5-96

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Solitaire 2 Revascularization Device, Solitaire Platinum Revascularization Device (Solitaire Revascularization Device)

    FDA 510(k)
    FDA Class 2 ·Neurology

    REAGENT, FIREFLY #395

    FDA 510(k)
    FDA Class 2 ·Hematology

    TITANIUM SCREW LOW PROFILE 5X40MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWT·November 18, 2016

    TITANIUM SCREW LOW PROFILE 5X40MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWT·November 18, 2016

    UNICEL® DXC 600I SYNCHRON® ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code MMI·February 27, 2013

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 5, 2014

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 8, 2011