BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    PAP-TRAY II (CATALOG #C600-2)

    FDA 510(k)
    FDA Class 1 ·Pathology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190776·Femoral Distal Cut Guide

    InterX

    FDA UDI
    HTK ENTERPRISES, INC.·00851894007428·The InterX Electrode Accessories are a critical...

    MILAGRO ADVANCE PEEK Interference Screw

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THERMASSAGE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PROLITE MESH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·April 11, 2014

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 26, 2012

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code GFA·July 14, 2010