BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    INSTRUCTION CHANGE FOR RIGHT ATRIAL/RAAF CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODEL 9500 ARGON, KRYPTON & DYE SURGICAL LASER SYS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

    FDA classification
    FDA Class 2 ·Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

    Laser, Ophthalmic

    FDA classification
    FDA Class 2 ·Laser, Ophthalmic