BEUDAMED
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    CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD BBL™ Selective Streptococcus Agar

    FDA UDI
    BECTON, DICKINSON AND COMPANY·10382902219344·Plate Select Streptococcus 20 Ea

    DePuy Mitek, Inc.

    FDA registration
    DePuy Mitek, Inc.·82 products·🇺🇸 United States

    TOMOTHERAPY TREATMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO MEDSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    1221934-1997-00026

    FDA Adverse Event
    Malfunction ·Product code GEI·September 17, 1997

    1221934-2018-55157

    FDA Adverse Event
    Malfunction ·October 31, 2018

    1221934-2017-10026

    FDA Adverse Event
    Malfunction ·January 20, 2017

    1221934-2018-50961

    FDA Adverse Event
    Malfunction ·July 2, 2018

    1221934-2018-50962

    FDA Adverse Event
    Malfunction ·July 2, 2018

    1221934-2012-00337

    FDA Adverse Event
    Injury ·DEPUY MITEK, A JOHNSON & JOHNSON COMPANY·December 10, 2012

    1221934-2018-53699

    FDA Adverse Event
    Malfunction ·August 7, 2018

    1221934-2018-52920

    FDA Adverse Event
    Malfunction ·August 23, 2018

    1221934-2018-52033

    FDA Adverse Event
    Malfunction ·July 23, 2018

    1221934-2018-54216

    FDA Adverse Event
    Malfunction ·July 26, 2018

    1221934-1997-00034

    FDA Adverse Event
    Injury ·Product code JDR·November 13, 1997

    1221934-2018-51386

    FDA Adverse Event
    Malfunction ·June 6, 2018

    1221934-2018-51387

    FDA Adverse Event
    Malfunction ·June 6, 2018

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MAI·December 27, 2017

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MAI·December 27, 2017