BEUDAMED
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    LABORIE FIBREOPTIC LIGHT CABLE

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517374592·CoRoent Small Contoured, 5L Open

    NA

    FDA UDI
    Richard Wolf GmbH·04055207043615·NEEDLE HOLDER Ø 5MM straight, WL 400mm, with i...

    MINIPEGASO COUGH, MINIPEGASO A-COUGH, MINIPEGASO A-COUG PERC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DYMEDIX REUSABLE RESPIRATORY EFFORT BELT SENSOR, MODEL 6015 AND DYMEDIX REUSABLE LIMB MOVEMENT SENSOR, MODEL 3100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FOUNDATION KNEE

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code JWH·May 30, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·November 20, 2012

    VITROS 350 CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·September 21, 2010

    PM3544 QUADRA RELIEVE and PM3562 QUADRA ALLURE MP These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·October 25, 2017