BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    SYNERGY ADJUSTABLE LENGTH ROD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169091498·ADJUSTER 3990057 CAPSTONE IR ADJ ONE

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377080608·RELINE C Cutter, Rod Ratcheting

    DJO Acetabular System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ON-CALL PLUS BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·March 5, 2013

    DST SERIES, EEA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDW·February 9, 2011

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 7, 2014

    Model 6149 Pacing Vector Selector Cable Switch for use with Pacing System Analyzers * Rx only * Contents Are Not Sterile * Manufactured by Remington Medical Incorporated, 6830 Meadowridge Court, Alpharetta, GA 30005, (770) 888-8520 or (800) 999-0057 * Distributed By: Guidant Corporation, 4100 Hamine Avenue North, St. Paul, MN 55112-5798 USA.

    FDA Recall
    Terminated ·Remington Medical Inc.·Product code DTA·August 31, 2005