BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    STAE

    FDA 510(k)
    FDA Class 2 ·Dental

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973092·posteriors; shade C1; size L; upper jaw

    RPMI-1640 MEDIUM NO. R7755 AUTO-MOD(TM) W.O/L-GLU.

    FDA 510(k)
    FDA Class 1 ·Hematology

    DECATHLON TWIN LUMEN HEMODIALYSIS CATHETER WITH SEPARATED TIPS, MODELS DE19SH24, DE23SH28, DE27SH32, DE31SH36, DE35SH40,

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·November 21, 2017

    LIFEVEST WCD 4000 SYS

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 5, 2014

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·February 21, 2013

    INRATIO

    FDA Adverse Event
    Other ·ALERE SAN DIEGO, INC.·Product code GJS·January 19, 2011