BEUDAMED
    6 results · 23ms · 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 Regulation: Us FDA ×

    Aperta NSE PTA Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HealthOST

    FDA 510(k)
    FDA Class 2 ·Radiology

    U0308 XENIUM 210G SYNTH HFDIALYZER

    FDA Adverse Event
    Injury ·NIPRO CORPORATION·Product code KDI·November 25, 2008

    HARMONIC SCALPEL

    FDA Adverse Event
    Injury ·ETHICON ENDO - SURGERY INC·Product code NLQ·September 2, 2011

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code NPT·July 23, 2013