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    LGM INTERNATIONAL INC.

    FDA registration
    LGM INTERNATIONAL INC.·5 products·🇺🇸 United States

    LGM PHARMA SOLUTIONS, LLC

    FDA registration
    LGM PHARMA SOLUTIONS, LLC·1 product·🇺🇸 United States

    KVP

    FDA UDI
    KVP International, Inc.·00742061700245·KVP Latex Gloves Medium (100 pk)

    NEPHELRATE ANTIPERUMS LGM

    FDA 510(k)
    FDA Class 2 ·Immunology

    RAPI/TEX-LGM KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    VENA TECH VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·B. BRAUN VENA-TECH·Product code DTK·May 12, 1998

    VENATECH

    FDA Adverse Event
    Death ·B. BRAUN MEDICAL INC.·Product code DTK·July 10, 2008

    AMERICAN PROTECTIVE PRODUCTS

    FDA UDI
    American Protective Products LLC·10850063932599·

    ELECSYS 2010

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 17, 2007

    INCSTAR EPSTEIN-BARR VIRAL CAPSID ANTIGEN (VCA) LGM ELISA KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    VENA TECH

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL, INC.·Product code DTK·August 19, 2004

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LGD·June 3, 2007

    INTEGRA 700

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 4, 2007

    VENA TECH - LGM

    FDA Adverse Event
    Death ·*·Product code DTK·March 2, 2006

    VENA TECH-LGM

    FDA Adverse Event
    Death ·VENA TECH B. BRAUN MEDICAL·Product code DTK·October 1, 1997

    VENA TECH VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·B. BRAUN VENA-TECH·Product code DTK·April 30, 1998

    VENATECH - LGM 30D/U VENA CAVA FILTER SYSTEM

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code DTK·July 24, 2007

    VENATECH - LGM 30D/U VENA CAVA FILTER SYSTEM

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL SAS·Product code DTK·December 4, 2007

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 2, 2009

    BRAUN VENA TECH LGM

    FDA Adverse Event
    Injury ·B BRAUN MEDICAL, INC.·Product code DTK·August 23, 1995