BEUDAMED
    14 results · 26ms · Sources: EU EUDAMED, US FDA

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    Hoffmann LRF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAREGUIDE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THERMO SCIENTIFIC MAS R DOA TOTAL

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 18, 2019

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 16, 2017

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017

    PUMP, INFUSION

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·February 3, 2023

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 18, 2018

    BD POSIFLUSH¿ NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 28, 2019

    PINN CAN BONE SCREW 6.5MMX20MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS12196·Product code NDJ·October 10, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·June 10, 2011

    ASCENSIA CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 9, 2008

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 17, 2017

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·July 15, 2024