BEUDAMED
    7 results · 19ms · 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 ×

    LIGHT GREEN

    FDA 510(k)
    FDA Class 1 ·Hematology

    Tyber Medical PT Interbody Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 13, 2014

    ACCURUS HIGH BRIGHTNESS ILLUMINATOR SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code MPA·October 14, 2010

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 13, 2012

    OPTIMA¿ MAX-XP TABLETOP ULTRACENTRIFUGE

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JQC·March 6, 2012