BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    MEDIFIX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848134980·Zip® Implant, 18 mm diam.

    DISPOSABLE TORQUE DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CHLORINATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2014

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·October 31, 2012

    NOT APPLICABLE (INCIDENT OCCURRED IN BCI WAREHOUSE)

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·August 24, 2010