BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    ANTIBODY TO RUBELLA VIRUS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ALCATEL-LUCENT TELEHEATH MANAGER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 2, 2014

    ACTIVE CORD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·October 16, 2012

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2010

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024