BEUDAMED
    20 results · 25ms · Sources: EU EUDAMED, US FDA

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    TITAN GEL ALKALINE PHOSPHATASE (HR)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MIZUHO ORTHOPEDIC SYSTEMS, INC.

    FDA registration
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·21 products·🇺🇸 United States

    TRIOS/STS SINGLE CHEST PAD

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·August 16, 2019

    NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ATOM 1 (MODEL: BRC 2200)

    FDA 510(k)
    FDA Class 2 ·Neurology

    PROAXIS SPINAL SURGERY TABLE (INT'L)

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·February 21, 2019

    MIZUHO OSI

    FDA Adverse Event
    Malfunction ·MIZUHO OSI·Product code JEA·May 25, 2016

    2921578-1997-00003

    FDA Adverse Event
    Malfunction ·Product code FQO·August 8, 1997

    2921578-2007-00001

    FDA Adverse Event
    Other ·Product code JEB·March 28, 2007

    2921578-2005-00002

    FDA Adverse Event
    Other ·Product code FWZ·July 12, 2005

    TRIOS/STS SINGLE CHEST PAD

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·August 16, 2019

    OXYGEN MASK

    FDA Adverse Event
    Other ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code BYG·November 15, 2010

    PILLOW

    FDA Adverse Event
    Other ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code FWZ·November 15, 2010

    CONSULTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NIK·December 13, 2010

    SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·January 18, 2013

    ACTIVA

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code MHY·July 9, 2014

    ADVANCED CONTROL BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·August 16, 2019

    HIP/THIGH/HINGE COVER

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code KME·April 12, 2019

    SHEARGUARD CHEST PAD COVERS

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code KME·April 12, 2019

    PROAXIS

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·January 18, 2019