BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    CHANGE OF CATHETER BODY MATERIAL (RADIO-OPAQUE NY)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Lacrimal Probe

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108703·MIYAKE LACRIMAL PROBE .65 AND .7MM

    Footmotion HammerToe

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTISTE MV SA

    FDA 510(k)
    FDA Class 2 ·Radiology

    M2A 38MM MOD HD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 13, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 8, 2010

    NELLCOR OXIMAX N-65

    FDA Adverse Event
    Malfunction ·SANMINA-SCI SYSTEMS·Product code DQA·December 11, 2012