BEUDAMED
    8 results · 18ms · 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.

    SAS SALMONELLA O GROUP D ANTIGEN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DILATING TIP TROCAR WITH STABILITY SLEEVE - 12MM DIAMETER

    FDA Adverse Event
    Injury ·Product code GCJ·June 20, 2006

    QUANTA LITE GLIADIN IGG II

    FDA 510(k)
    FDA Class 2 ·Immunology

    RECON system - MPJ-Plates

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RUNWAY GUIDE CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·May 8, 2013

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code DXY·February 9, 2013

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 23, 2014

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 7, 2011