BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACROMED BUTTON SPINAL WIRE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NON-STERILE LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    KENDALL CURITY SUCTION CATHETERS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 25, 2014

    CRYSTALENS

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code NAA·November 4, 2010

    DCP 2 6HO L32 SST

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code LXT·January 3, 2013

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020