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

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    MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112892·CORNEAL TREPHINE BLADE7.0MM

    OSSEOTITE® IMPLANT 3.75 X 11.5MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·August 6, 2021

    G-FREEZEKIT BLAST

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CAPSURE PS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OSSEOTITE® IMPLANT 3.75 X 10MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·August 6, 2021

    ONE TOUCH PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·November 4, 2008

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·September 2, 2011

    JOURNEY

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·July 17, 2013

    BSM-1733A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·July 10, 2018