BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    ALL-HANDS MEDICAL SUPPLY SUTURE REMOVAL

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    MODIFICATION TO PROTEX STABILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OCT-Camera

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CONTINUUM LONGEVITY CONSTRAINED LINER, KK 32 X 56

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·October 23, 2018

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 2, 2014

    CIRCUIT NEONATE 4FT HTD W/ 30/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BZE·November 21, 2012

    SOLOIST SINGLE NEEDLE ELECTRODEELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code GEI·September 23, 2010

    FEMORAL STEM 12/14 NECK TAPER PLASMA SPRAYED PRESS-FIT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 24, 2021