BEUDAMED
    7 results · 37ms · 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.

    PHARMACIA IGE EIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228730771·GC Initial™ AL Translucent Mod. TM-04, 20g

    Cavetto-SA Cervical Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOLUMIN. SCREENING FOR BACT. BY ATP A.

    FDA 510(k)

    PENUMBRA SYSTEM 5MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·June 13, 2014

    MODULAR HEAD COMPONENT 32MM HEAD DIAMETER -3MM NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·October 18, 2010

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·December 13, 2012