BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ASP-100, MODEL 2100

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    GOPHER GOLD CATHETER, MODEL 5620

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Pegasus System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·December 17, 2019

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·December 17, 2019

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·March 6, 2013

    ADAPTER SLEEVES 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·August 8, 2014

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011