BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    MERIVAARA PATIENT TROLLEY - MODEL #416

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LIAISON® EA IgG and LIAISON® EA IgG Serum Control Set

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DMS 300-2, 300-3 AND 300-4

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLUM A + DRIVER NEW

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 20, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 9, 2010

    STERRAD 100NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·December 10, 2012

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

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