BEUDAMED
    6 results · 34ms · 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 ×

    S4 MONOAXIAL SCREW 8.0X45MM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code KWP·February 23, 2006

    PERSONA NATURAL TIBIA TRABECULAR METAL TWO-PEG POROUS FIXED BEARING LEFT SIZE G

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MBH·February 21, 2017

    HEARTWARE VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·May 20, 2013

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 10, 2011

    VITROS IMMUNODIAGNOSTICS PRODUCTS ANTI-HIV 1 + 2 REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MTL·August 14, 2008

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·January 28, 2016