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

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    LACTOPLATE

    FDA 510(k)
    FDA Class 1 ·Immunology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209110858·

    DeGen Medical Latitude-C AM Cervical Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Lite Touch

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OT VERIO SYNC METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 30, 2012

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·September 25, 2010

    Knee Arthroscopy Pack , part number AMS2610(A Knee Arthroscopy Pack, part number AMS3236(A Knee Arthroscopy Pack, part numbre AMS3860

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015