BEUDAMED
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    H-I-M-TEST FOR DETECTING HUMAN CHOR. GON

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·March 24, 2020

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·March 24, 2020

    ABGII MODULAR LONG NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·April 28, 2020

    ABGII. MODULAR STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·April 28, 2020

    RAD-G

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·October 12, 2025

    GON Infinity TL RP Solid abutment blue, 6°, H 7.0 mm

    FDA UDI
    Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50810961·TL RP Solid abutment blue, 6°, H 7.0 mm for GON...

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Other ·ABBOTT LABORATORIES·Product code JJE·June 19, 1998

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 6, 2024

    VENFLON I 20GA 1.0 MM X 32MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·November 12, 2020

    C-GON / NUTRISAFE 5 ML FEEDING SYRINGE

    FDA Adverse Event
    Malfunction ·VYGON·Product code FPD·June 9, 2017

    DOW CORNING

    FDA Adverse Event
    Injury ·DOW CORNING CORP.·Product code FTR·October 21, 1998

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 24, 2008

    GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic images of the skull, spinal column, chest, abdomen, extremities and other body parts in patients of all ages.

    FDA Enforcement
    Class II ·Terminated·GE Healthcare, LLC·August 27, 2014

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 24, 2008

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·September 10, 2008

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 22, 2023

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 27, 2008

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 27, 2008

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 19, 2008