BEUDAMED
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    PULPDENT POLYAMIDE DENTIN LINER

    FDA 510(k)
    FDA Class 1 ·Dental

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909112852·REVELATION DIAMOND 862-012VF - 5 PACK

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111446696·SAIRGES TENACULUM FORCEPS 9 IN

    Spine & Trauma Navigation

    FDA 510(k)
    FDA Class 2 ·Neurology

    AQUAMANTYS 3 PUMP GENERATOR, BIPOLAR SEALER, BIPOLAR SEALER WITH CUTTING

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 11, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 22, 2010

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·July 2, 2014

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018