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

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    CARDIOPULMONARY BYPASS ACCESSORY EQUIP.

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    PHASE II GBM IGG ANTIBODY EIA TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    RE / STASIS (TM) GINGIVAL RETRACTION PASTE

    FDA 510(k)
    FDA Unclassified ·Unknown

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·November 13, 2020

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·November 9, 2020

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 2, 2015