BEUDAMED
    9 results · 24ms · 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.

    ORTHO FACTOR XI DEFICIENT PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    PENTAX Medical ENT Video Imaging System

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BONEVUE

    FDA 510(k)
    FDA Class 2 ·Radiology

    TEGO CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·August 10, 2015

    SAGITTAL SAW ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·June 19, 2014

    TRANSTAR

    FDA Adverse Event
    Malfunction ·HILL-ROM·Product code FPO·October 15, 2010

    VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code DYX·December 21, 2012

    TEGO CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·September 2, 2016

    TEGO CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·September 2, 2016