BEUDAMED
    7 results · 21ms · 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 ×

    ELECTRICAL NERVE STIMULATION(TENS) ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    LONG NAIL KIT R2.0, TI, LEFT GAMMA3 11 X 360MM X 12

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 6, 2012

    Remedy® Shoulder Spacer

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUPERCATH V

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

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·June 5, 2014

    L COMPRESSION PROFILE PLATE, T-SHAPE, BEVELLED, NA

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code HRS·November 12, 2012

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·September 29, 2010