BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NextAR™ Spine Platform

    FDA 510(k)
    FDA Class 2 ·Neurology

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114032·GIANNETTI MODIFIED J-CANNULA (PK/10)

    MOSAIQ Oncology Information System

    FDA 510(k)
    FDA Class 2 ·Radiology

    CANDELA GENTLEYAG FAMILY OF LASER SYSTEMS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·November 18, 2008

    UNIVERSAL DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·July 22, 2011

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 18, 2013