BEUDAMED
    7 results · 33ms · 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 FDA Adverse Event ×

    COBAS EGFR MUTATION TEST

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS, INC.·Product code OWD·January 29, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 10, 2013

    CONEXA

    FDA Adverse Event
    Injury ·LIFECELL CORPORATION·Product code FTM·July 13, 2011

    FOX SV PTA CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR SWITZERLAND·Product code LIT·September 12, 2008

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·December 10, 2018

    ZENITH TX2 DISSECTION ENDOVASCULAR GRAFT STRAIGHT COMPONENT

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code MIH·November 11, 2024

    COBAS EGFR MUTATION TEST

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code OWD·January 14, 2015