BEUDAMED
    19 results · 54ms · Sources: EU EUDAMED, US FDA

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    Thumper

    FDA UDI
    MICHIGAN INSTRUMENTS, LLC·00860682000114·External Cardiac Compressor - Thumper Model 100...

    Life-Stat

    FDA UDI
    MICHIGAN INSTRUMENTS, LLC·00860682000121·External Cardiac Compressor - Life-Stat Model 1...

    Thumper

    FDA UDI
    MICHIGAN INSTRUMENTS, LLC·00860682000107·External Cardiac Compressor - Model 1007CCMII

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·October 6, 2021

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·October 26, 2021

    LIFE-STAT

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·August 1, 2023

    LIFE-STAT

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·May 20, 2022

    LIFE-STAT

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·October 16, 2018

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·November 28, 2018

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·October 5, 2021

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·October 6, 2021

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·May 15, 2019

    LIFE-STAT

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·July 31, 2024

    LIFE-STAT

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·March 25, 2024

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·January 27, 2025

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·January 8, 2020

    LIFE-STAT

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·September 17, 2019

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, LLC·Product code DRM·November 6, 2019

    Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for total and partial knee arthroplasty. Part of the Signature Personalized Patient Care System.

    FDA Recall
    Terminated ·Materialise N.V. 15 Technologielaan Heverlee Belgium·Product code OSF·September 23, 2015