BEUDAMED
    38 results · 65ms · Sources: EU EUDAMED, US FDA

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    MSK Precision Products, Inc.

    FDA registration
    MSK Precision Products, Inc.·5 products·🇺🇸 United States

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 23, 2018

    ATLANTIS(R) Anterior Cervical Plate System Screw Caddy; Self Tapping Variable Screw Caddy (176-513). Medtronic Sofamor Danek USA, Inc. This instrument is a precision device which incorporates a measuring function.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code XLH·July 6, 2011

    ATLANTIS(R) Anterior Cervical Plate System Screw Caddy; Self Drilling Fixed Screw Caddy (976-516). Medtronic Sofamor Danek USA, Inc. This instrument is a precision device which incorporates a measuring function.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code XLH·July 6, 2011

    VITROS 5600 INTEGRATED SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·March 6, 2019

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 28, 2018

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 30, 2018

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·April 9, 2018

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·July 11, 2024

    MEGADYNE

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·December 17, 2014

    A1A-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 26, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 6, 2018

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·April 16, 2018

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 30, 2018

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 29, 2018

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 31, 2018

    CARELINK PRO ONLINE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code PHV·August 8, 2023

    DAVINCI SI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·July 20, 2023

    RiteAid Glucose Monitoring System; Recalling Firm/Manufacturer: Abbott Diabetes Care, Inc., 1360 South Loop Road, Alameda, CA 94502

    FDA Recall
    Terminated ·Abbott Laboratories Medisense Products·Product code NBW·June 7, 2005

    Liberty Glucose Monitoring System; Recalling Firm/Manufacturer: Abbott Diabetes Care, Inc., 1360 South Loop Road, Alameda, CA 94502

    FDA Recall
    Terminated ·Abbott Laboratories Medisense Products·Product code NBW·June 7, 2005