BEUDAMED
    10 results · 29ms · 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 ×

    HOWMEDICA PREMIUM FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SeaSpine Spacer System - Redondo™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981045142·Redondo Trial 26mm x 24mm x 17mm, Lordotic

    SURE-CLOSURE 75MM SKIN STRETCHING SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TDX/TDXFLX & TDXFLX THEOPHYLLINE MONOCLONAL II

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 30, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 13, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 15, 2014

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·April 9, 2014

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·March 24, 2014

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·February 20, 2014