BEUDAMED
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    DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION

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

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122819·K-WIRE - DOUBLE TROCAR 0.6mm DIA x 100mm

    Bausch & Lomb Incorporated

    FDA registration
    Bausch & Lomb Incorporated·27 products·🇺🇸 United States

    PICCOLO TRGLYCERIDES-CAPILLARY TEST SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    STERISHARP 3-GALLON RSDC, MODEL RSDC3G

    FDA 510(k)
    FDA Class 2 ·General Hospital

    1920664-2002-00001

    FDA Adverse Event
    Injury ·Product code ---·January 15, 2002

    1920664-2002-00002

    FDA Adverse Event
    Injury ·Product code ---·January 15, 2002

    1920664-2007-00488

    FDA Adverse Event
    Injury ·Product code HQL·April 26, 2007

    1920664-2003-00137

    FDA Adverse Event
    Injury ·Product code ---·March 18, 2003

    1920664-1997-00200

    FDA Adverse Event
    Malfunction ·Product code HQE·April 14, 1997

    1920664-1997-00185

    FDA Adverse Event
    Injury ·Product code HQE·April 11, 1997

    1920664-1996-00833

    FDA Adverse Event
    Injury ·Product code HQC·November 14, 1996

    1920664-1996-00832

    FDA Adverse Event
    Injury ·Product code HQC·November 14, 1996

    1920664-1996-00810

    FDA Adverse Event
    Injury ·Product code HQC·November 6, 1996

    1920664-1998-00163

    FDA Adverse Event
    Product code HQE·August 6, 1998

    1920664-2006-00050

    FDA Adverse Event
    Injury ·Product code HQC·May 22, 2006

    1920664-2006-00049

    FDA Adverse Event
    Injury ·Product code HQC·May 22, 2006

    1920664-2001-00043

    FDA Adverse Event
    Injury ·Product code MOE·December 12, 2001

    1920664-2000-00002

    FDA Adverse Event
    Injury ·Product code HQC·March 7, 2000

    1920664-2001-00001

    FDA Adverse Event
    Injury ·Product code HQC·January 4, 2001