BEUDAMED
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    ANTIGENZ CHLAMYDIA

    FDA 510(k)
    FDA Class 2 ·Neurology

    FLI Twin

    FDA UDI
    Rmo, Inc.·00885797503565·FLI(R) TWIN ROTH .022 HK345 5-5 20 BKTS

    NO PROFILE

    FDA UDI
    Biomet Sports Medicine, LLC·00880304420731·

    ADD'L USES FOR THE KODAK SURECELL CHLAMYDIA KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    VS-1 LEAD EXT. 033-302, 4.75MM 033-260, 033-458

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·January 6, 2021

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code JJE·March 19, 2020

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·March 11, 2019

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·June 14, 2021

    ARCHITECT C4000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·July 23, 2024

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 16, 2019

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 15, 2019

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·February 9, 2022

    ARCHITECT C8000 PROCESSING MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code JJE·April 28, 2020

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·April 17, 2023

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·March 24, 2019

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·April 26, 2019

    ISOFLEX S

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·November 19, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 1, 2014