BEUDAMED
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    MMI-Micro

    FDA UDI
    EasyMed Instruments Co., Ltd.·06942808291010·MMI-Micro is used to provide symptomatic pain r...

    MMI NORTH AMERICA, INC.

    FDA registration
    MMI NORTH AMERICA, INC.·2 products·🇺🇸 United States

    MMI App for iOS

    FDA UDI
    Modular Medical, Inc.·00850037806010·iOS smartphone application for MODD1 Insulin De...

    BIOSOUND MMI ULTRASOUND

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MMI/GAELTEC CATHETER INTRAUTERINE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MMI/GAELTEC CATHETER TIP PRESSURE

    FDA 510(k)
    FDA Class 2 ·Neurology

    MMI/GAELTEC CATHETER TIP TRANSDUC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AlignRT Plus

    FDA UDI
    VISION RT LIMITED·05056190500306·

    QUICK C DOUBLE CONTRAST BARIUM ENEMA TUBE

    FDA Adverse Event
    Injury ·MMI·Product code FGD·July 6, 1995

    MMI/GAELTEC CATHETER TIP PRESS. TRANSDU

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

    MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    MULTIPLACE HYPERBARIC SYSTEM, MODEL MMI HYPERBARIC CHAMBER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TIP - DUAL FLEX

    FDA Adverse Event
    Injury ·MMI INC.·July 1, 1993

    1.8 mm Y-Knot® Disposable Instrument Kit

    FDA UDI
    Conmed Corporation·20653405990779·1.8 mm Y-Knot® Disposable Instrument Kit with S...

    1.8 mm Y-Knot® Disposable Instrument Kit

    FDA UDI
    Conmed Corporation·20653405990762·1.8 mm Y-Knot® Disposable Instrument Kit with C...

    UNKNOWN MMI TITANIUM IMPLANT

    FDA Adverse Event
    Injury ·MEMOMETAL TECHNOLOGIES SA·Product code HTY·September 20, 2011

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·May 29, 2019

    MINIMED INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MINIMED, INC.·Product code LZG·September 12, 2001

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·September 19, 2019

    ESPRIT VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·March 15, 2018