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

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    THE KEELER ALL PUPIL INDIRECT OPHTHALMOSCOPE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209127696·

    THEOFAST TEST KIT FOR QUANTITATIVE THEO

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Wearable Breast Pump (Model S39)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ULTRATHANE DAWSON-MUELLER MAC-LOC LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GBO·October 9, 2018

    LEAD MODEL 304

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·June 6, 2014

    MAXPLUS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code FPA·October 24, 2012

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·September 3, 2010