BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    DMA OXYGEN MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209111664·

    Dukal Crepe Paper Sterilization Wrap

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMPLANTIUM ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    BD DISC CEFTAZIDIME CAZ-30 JAPAN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code JTN·January 18, 2022

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 6, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 5, 2010

    PCA EMPTY STERILE

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC·Product code MEA·November 27, 2012

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015