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    Minnesota Medical Technologies

    Manufacturer
    🇺🇸 United States·1 Basic UDI-DI·3 Devices·1 Importer

    MINNESOTA MEDICAL TECHNOLOGIES

    FDA registration
    MINNESOTA MEDICAL TECHNOLOGIES·1 product·🇺🇸 United States

    Minnesota Medical Technologies Fecal Incontinence Insert (My Miracle)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Navina Fecal Incontinence Insert, Starter Pack, 10/Box

    Device
    EU MDR · Eu Md Class 2a ·Minnesota Medical Technologies·On the market·12 countries

    Navina Fecal Incontinence Insert, Size Large, 30/Box

    Device
    EU MDR · Eu Md Class 2a ·Minnesota Medical Technologies·On the market·12 countries

    Navina Fecal Incontinence Insert, Size Standard, 30/Box

    Device
    EU MDR · Eu Md Class 2a ·Minnesota Medical Technologies·On the market·12 countries

    StaySure

    FDA UDI
    Minnesota Medical Technologies Corporation·00865453000355·Fecal Incontinence Insert, StaySure, Evaluation...

    StaySure

    FDA UDI
    Minnesota Medical Technologies Corporation·00865453000348·Fecal Incontinence Insert, StaySure, 30-Pack, L...

    StaySure

    FDA UDI
    Minnesota Medical Technologies Corporation·00865453000324·Fecal Incontinence Insert, StaySure, Starter Pack

    StaySure

    FDA UDI
    Minnesota Medical Technologies Corporation·00865453000331·Fecal Incontinence Insert, StaySure, 30-Pack, S...

    StaySure

    FDA UDI
    Minnesota Medical Technologies Corporation·00865453000379·Fecal Incontinence Insert, StaySure, 10-Pack, L...

    StaySure

    FDA UDI
    Minnesota Medical Technologies Corporation·00865453000362·Fecal Incontinence Insert, StaySure, 10-Pack, S...

    HEMOLUNG RAS

    FDA Adverse Event
    Injury ·ALUNG TECHNOLOGIES, INC.·Product code QOH·February 24, 2023

    HEMOLUNG RAS

    FDA Adverse Event
    Injury ·ALUNG TECHNOLOGIES, INC.·Product code QOH·February 24, 2023

    HEMOLUNG RAS

    FDA Adverse Event
    Injury ·ALUNG TECHNOLOGIES, INC.·Product code DQR·January 18, 2023

    Fecal Incontinence Insert

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Minnesota Medical Technologies·3 devices

    AMPLATZER DUCT OCCLUDER II

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code MAE·October 10, 2023

    AMPLATZER VASCULAR PLUG II

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code KRD·October 10, 2023

    AMPLATZER VASCULAR PLUG II

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code KRD·October 10, 2023

    Nonin Model 7600B cerebral oximeter pod. Used with the Nonin Model 7600 Regional Oximeter with Equanox Technology and Bluetooth Wireless Technology. Nonin Medical, Inc., 13700 First Avenue North, Plymouth, Minnesota 55441-5443 USA.

    FDA Recall
    Terminated ·Nonin Medical, Inc·Product code MUD·October 23, 2009