BEUDAMED
    9 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 ×

    MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Up&Up

    FDA UDI
    TARGET CORPORATION·06945397906242·Hot + Cold Gel Bead Compress with Strap) - up & up

    NEUROPACK MICRO, MODEL MED-9100A SERIES

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LATERAL PIVOT INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MESH, SURGICAL

    FDA Adverse Event
    Injury ·W. L. GORE AND ASSOCIATES, INC.·Product code FTM·August 12, 2023

    LINEAR 3-6

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 22, 2024

    DELTA CERAMIC FEM HD 36/ 0MM (T1)

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 22, 2013

    REAGENT RED BLOOD CELLS BIOTESTCELL 1 & 2

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·April 7, 2011

    CONTOUR TEST STRIPS (50)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·July 1, 2008