BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    KODAK RP X-OMAT PROCESSOR MODEL M6B

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEM W/SPINNER SALTS POWDER MEDIUM

    FDA 510(k)
    FDA Class 1 ·Hematology

    FILL HOSE SAFETY ADAPTER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 9, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 6, 2010

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 3, 2012

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020