BEUDAMED
    8 results · 31ms · 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.

    Elastic Impression Material

    FDA 510(k)
    FDA Class 2 ·Dental

    Disposable Hemodialysis Access Catheter Set

    FDA UDI
    Guangdong Baihe Medical Technology Co., Ltd.·06938634496408·

    HD BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HAUSTED POWERTRAN SERIES STRETCHER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CAPTURE-R READY SCREEN 3

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·September 9, 2011

    8010042-2008-00141

    FDA Adverse Event
    Malfunction ·Product code CBK·August 29, 2008

    2520274-2013-04577

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 22, 2013

    CERELINK ICP EXT CABLE

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code GWM·August 2, 2022