BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    AVS PL PEEK SPACERS, MODELS 48351XXX AND 48353XXX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO M2376A DEVICELINK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Sterilizer, Steam

    FDA classification
    FDA Class 2 ·Sterilizer, Steam

    Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

    FDA classification
    FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)