BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    IMPULSE 3000 DEFIBRILLATOR ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981031237·11mm Hollywood Trial, Lordotic

    PBC IV SET VENTED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NA ALPHA 1 MICROGLOBULIN KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    AUTOSOFTÂ XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 3, 2010

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 7, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014