BEUDAMED
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    GRAM NEGATIVE AND POSITIVE MIC/COMBO PANELS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756571159·SURGICAL PACK

    ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SERALYZER DRUG ASSAY CONTROL SERUM

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    UNSPECIFIED BIS PRODUCT

    FDA Adverse Event
    Injury ·CELESTICA ELECTRONICS·Product code GXY·June 9, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 3, 2010

    COROX OTW-L 85-BP

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code OJX·December 21, 2012

    GYC-1000

    FDA Adverse Event
    Malfunction ·NIDEK CO., LTD.·Product code HQF·June 18, 2015