BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 1 ·Radiology

    IMPLANT: HA, SPLINE, 10MM, 3.25

    FDA Adverse Event
    Injury ·SULZER CALCITEK·Product code DZE·November 12, 1998

    ENSEAL TRIO TISSUE SEALING DEVICE

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

    MODIFICATION TO STANDARD HUMAN PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 1, 2024

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·January 18, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    INTEGRITY DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 9, 2014