BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD BBL™ Sensi-Disc™ Fosfomycin 200 µg

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902317098·BD BBL™ Sensi-Disc™ Fosfomycin 200 µg

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694022095·FPS 3.5/4.0mm Countersink

    SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Biotres

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 11, 2024

    TRIDENT 0 DEG X3 INSERT 32MM HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 1, 2019

    QUICK COUPLING FOR KIRSCHNER WIRES

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·November 6, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

    PARIETEX UGYTEX PP POSTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTP·July 12, 2013