BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    FLOOR LINE INSTRUMENTS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SYNCHRON® AMYLASE (AMY) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JFJ·September 21, 2010

    Intertape Polymer Inc., Type 1 Bismuth Process Indicator Steam Sterilization Tape

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TINA-QUANT CERULOPLASMIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 21, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code NVY·October 15, 2012

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 10, 2010