BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    FOUNDATION POROUS HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALIF

    FDA UDI
    Nuvasive, Inc.·00887517837639·ALIF Blade, 80mm Standard

    DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ELECTRODE, ELECTROSURGERY

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·June 25, 1997

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL MANUFACTURING CORPORATION·Product code MVK·August 5, 2015

    PROLIFT PELVIC FLOOR REPAIR

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

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014