BEUDAMED
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    Qualitative And Quantitative Hepatitis B Virus Antibody Assays

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLISA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLISA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLISA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLISA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLISA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·MONOLISA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLOSA ANTI-HBC EIA

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·BIO-RAD MONOLISA ANTI-HBC EIA

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496060031·CURVY 70 OPAQUE, SIZE M-XL, NERO, GRADUATED COM...

    5MS

    FDA UDI
    In2Bones USA, LLC·00817906029673·5MS, T15 DRIVER, CANNULATED, AO

    5MS

    FDA UDI
    In2Bones USA, LLC·00810021861876·5MS T15 Driver, Cannulated, Sterile, Single-Use

    Durable BP Cuff

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935104070·

    Xsert Lumbar Expandable Interbody System

    FDA UDI
    Xtant Medical Holdings, Inc.·M697T0920600311·15mm x 10mm x 32mm TRIAL

    DEPUY MODULAR M HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIMILAR DEVICE BNI75TCDDH, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2017

    SIMILAR DEVICE DI7TCBLRT, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 9, 2015

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 19, 2013

    CLINICAL CHEMISTRY BILIRUBIN CALIBRATOR

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JIX·June 12, 2008

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 15, 2011

    THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·January 14, 2014