BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Finger Pulse Oximeter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304255289·

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·October 18, 2002

    SONIC-STIM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UNISTRIP 1

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    2124215-2011-08512

    FDA Adverse Event
    Injury ·GUIDANT PUERTO RICO BV·Product code NVN·July 15, 2011

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·June 11, 2013

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·September 16, 2008