BEUDAMED
    7 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    CardioPhase® hsCRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    MICRUS MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRIATHLON TRITANIUM METAL-BACKED PATELLA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REPROCESSED DECANAV EP CATHETER, F CURVE

    FDA Adverse Event
    Injury ·STERILMED, INC.·Product code NLH·September 4, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 6, 2014

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code MIH·August 25, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·July 18, 2013