BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    STEINMAN PIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNCHRON URIC ACID

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code KNK·June 10, 2011

    VOLCANO ANGIO-IVUS MAPPING (AIM) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Burn-out Cylinder and Angled Screw Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE

    FDA Adverse Event
    Malfunction ·MEDELA INC·Product code HGX·June 24, 2014

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·February 11, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 13, 2011

    CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026