BEUDAMED
    8 results · 20ms · 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 ×

    ASCENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASCENT SYSTEM-BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·December 28, 2016

    AWBAT-S, AWBAT-D, AWBAT-M

    FDA 510(k)
    FDA Unclassified ·Unknown

    Fit SA

    FDA 510(k)
    FDA Class 2 ·Dental

    CADD-LEGACY® PCA AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD INC.,·Product code MEA·March 29, 2016

    2008K HEMODIALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014

    MSERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 31, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·February 9, 2011