BEUDAMED
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    VITEK 2 AST ST MOXIFLOXACIN, VITEK 2 AST STREPTOCOCCUS MOXIFLOXACIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Bernafon

    FDA UDI
    Bernafon AG·05711584050866·CA5 ITED, WL L BE CARISTA 5

    QUANTA SYSTEM S. P. A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·December 9, 2014

    PROVU (TM) DENTAL X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    DIMENSION PROCAINAMIDE (PROC) FLEX REAGENT CARTRIDGE METHOD, MODEL DF110

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2024

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 1, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·May 1, 2013

    6.5 CANCELLOUS BONE SCREW 25MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code HWC·June 10, 2011