BEUDAMED
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    MAYO CLINIC BC-10 1.5T

    FDA 510(k)
    FDA Class 2 ·Radiology

    MAYO CLINIC BC-10 3.0T

    FDA 510(k)
    FDA Class 2 ·Radiology

    642E Centrifuge, Mayo Clinic

    FDA UDI
    DRUCKER DIAGNOSTICS·00810052861319·General purpose laboratory centrifuge for sampl...

    MAYO CLINIC GENEGUIDE HELIX

    FDA Adverse Event
    Malfunction ·UNK·Product code PTA·March 20, 2020

    MAYO CLINIC ELBOW PLATES

    FDA Adverse Event
    Injury ·ACUMED·Product code HRS·November 21, 2002

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code LRO·December 30, 2016

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 25, 2025

    CARDIOQUIP MODULAR COOLER HEATER

    FDA Adverse Event
    Malfunction ·CARDIOQUIP, LLC·Product code DWC·September 15, 2023

    MAYO CLINIC CONGRUENT BONE PLATE SYSTEM

    FDA Adverse Event
    Other ·ACUMED·Product code HRS·December 20, 2005

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code OHD·April 3, 2025

    STYLE 133MX TISSUE EXPANDER

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code LCJ·January 14, 2025

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·April 29, 2025

    ACUMED MAYO CLINIC CONGRUENT BONE PLATE SYSTEM

    FDA Adverse Event
    Other ·ACUMED·Product code HRS·August 3, 2005

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·March 2, 2025

    VITEK® 2 ANAEROBIC AND CORYNEBACTERIA IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, INC.·Product code JSP·April 9, 2015

    POWERPORT CLEARVUE ISP IMPLANTABLE PORT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD) -3006260740·Product code LJT·September 24, 2022

    POWERPORT ISP IMPLANTABLE PORT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD) -3006260740·Product code LJT·September 24, 2022

    POWERPORT ISP IMPLANTABLE PORT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD) -3006260740·Product code LJT·September 24, 2022

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·September 21, 2020

    VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC IGM REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code LOM·March 22, 2023