BEUDAMED
    10 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 ×

    MAR BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228751451·GC Initial™ Zr-FS Inside IN-45 Havanna, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556708436·GC Initial™ Zr-FS Inside IN-45 Havanna, 20g

    Centerline Thoracolumbar Spinal System

    FDA UDI
    Life Spine, Inc.·00190837065034·4.75mm x 145mm CoCr Rod, Prelordosed, No Hex End

    G-Beam Fusion Beaming System

    FDA UDI
    ORTHOFIX SRL·18053504360650·G-BEAM STAINLESS STEEL FUSION BEAM L145MM D5.4M...

    MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EXTERNAL Y VALVE 5C4198

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 3, 2013

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 19, 2010

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·December 12, 2012