BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    DualCap

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814572·GENUMEDI SAND SIZE VI

    QUADRANT UNIT-1-BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS

    FDA 510(k)
    FDA Unclassified ·Unknown

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 24, 2013

    CONTINUUM TM SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LZO·September 23, 2014

    TRANSPORT SERIES

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·June 20, 2011

    Cobe Optima XP Hollow Fiber Membrane Oxygenator, Non-Sterile, Catalog Number 436422974, COBE Cardiovascular, Inc.. (shipped International only for use in Heart/Lung packs)

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code DTZ·June 26, 2006