BEUDAMED
    9 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 ×

    MODEL 1240, SMALL E NET

    FDA 510(k)
    FDA Class 2 ·Neurology

    PROULTRA ENDO TIPS

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code ELC·June 8, 2006

    SYNCHRON URIC ACID

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code KNK·June 10, 2011

    HemosIL D-Dimer HS

    FDA 510(k)
    FDA Class 2 ·Hematology

    MODEL MI 44 TYMPANOMETER

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

    AZO

    FDA Adverse Event
    Other ·SIEMENS DIAGNOSTICS, INC.·Product code CEN·July 12, 2012

    HIRES 90K IMPLANT

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·June 27, 2014

    CAREASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·January 16, 2013

    LCS COMPLETE FEM CEM R LG

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code NJL·January 11, 2011