BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ROCCIA® PLIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARMADA 35/35LL PTA CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANYRAY PORTABLE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 21, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 28, 2011

    CYLOS DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO.·Product code DXY·September 25, 2008

    HUMAPEN ERGO, BURGUNDY/CLEAR

    FDA Adverse Event
    Injury ·ELI LILLY AND CO.·Product code FMF·February 7, 2008

    HUMAPEN ERGO, BURGUNDY/CLEAR

    FDA Adverse Event
    Injury ·ELI LILLY AND CO.·Product code FMF·February 12, 2008