BEUDAMED
    6 results · 18ms · 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 ×

    CYTOPLAST REGENTEX TITANIUM 250

    FDA 510(k)
    FDA Class 2 ·Dental

    BRK TRANSSEPTAL NEEDLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Firlit-Kluge Urethral Stent, Koyle Diaper Stent, Zaontz Urethral Stent

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PROLIFT +M PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTP·February 21, 2013

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Death ·NXSTAGE MEDICAL, INC.·Product code KDI·January 21, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014