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

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    Filters Regulation: Us FDA ×

    PLASTIC PORT IMPLANTABLE VENOUS ACCESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197751·AK3 PS-C Insert Trial Size 2, 16mm

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024157415·

    STERILE WATER SOLUTION CATALOG # 10000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HAEMOPHILUS TEST MEDIUM (HTM)AGAR

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CATH TEMPO AQUA 4F

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQO·March 8, 2013

    FLEXICAP DISCONNECT CAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·February 17, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 8, 2014