BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    REPLACE-A-TIP RECHARG. LOW TEMP.

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TRC-NW8F PLUS NON-MYDRIATIC RETINAL CAMERA

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DISPOSABLE COLORED VINYL SYNTHETIC EXAM GLOVE, POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    EM ESPE SCOTCHBOND UNIVERSAL

    FDA Adverse Event
    3M DEUTSCHLAND GMBH·Product code KLE·May 15, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·October 19, 2012

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (LARGE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 13, 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