BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    Carestation 620/650/650C

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BONE SCREW, CORTICAL

    FDA UDI
    Biomet Orthopedics, LLC·00887868004766·

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837088941·

    Canaveral®

    FDA UDI
    FLOSPINE LLC·B183115150700·Reduction Monoaxial Screw, 10.5mm x 70mm

    HYPERGLIDE AND HYPERFORM OCCLUSION BALLOON SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AVL HINGE KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FRESENIUS 8

    FDA Adverse Event
    Injury ·FRESENIUS·Product code KDI·August 6, 1997

    PENUMBRA SMART COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

    ADAPTA VDD

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code NVZ·June 7, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 6, 2011

    WORLEY-STD

    FDA Adverse Event
    Malfunction ·THOMAS MEDICAL PRODUCTS, INC.·Product code DYB·September 3, 2008