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

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    Filters Regulation: Us FDA ×

    Steripack cases and Tray Systems

    FDA 510(k)
    FDA Class 2 ·General Hospital

    I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5

    FDA 510(k)
    FDA Class 2 ·Radiology

    CORVIS ST

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2020

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 13, 2008

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 27, 2013

    PROVISIONAL LINER LOCKING SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LXH·July 22, 2011

    CD HORIZON ASTUTE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code NQP·April 16, 2021