BEUDAMED
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    FDA UDI
    KEY SURGICAL, INC.·10849771047381·Sterilization Wrap, 500 Weight, 45-inch x 45-in...

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771047374·Sterilization Wrap, 500 Weight, 30-inch x 30-in...

    STAT PROFILE

    FDA UDI
    NOVA BIOMEDICAL CORPORATION·00385480489065·Stat Profile pHOx Ultra/CCX Chemistry Controls ...

    Integra® Ruggles®-Redmond™

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780177401·Integra® Ruggles®-Redmond™ Fukushima-Day Retrac...

    Cardinal Health Costa Rica, S.A.

    FDA registration
    Cardinal Health Costa Rica, S.A.·2 products·🇨🇷 Costa Rica

    BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER

    FDA registration
    MedXL·2 products·🇺🇸 United States

    Spectrum Central Venous Tray Double Lumen Polyurethane Catheter Minocycline/Rifampin Impregnated

    FDA registration
    Cook Incorporated·2 products·🇺🇸 United States

    ARGON MEDICAL DEVICES INC.

    FDA registration
    ARGON MEDICAL DEVICES INC.·2 products·🇺🇸 United States

    Cardinal Health 200, LLC

    FDA registration
    Cardinal Health 200, LLC·2 products·🇺🇸 United States

    SPECTRUM SILICONE CATHETER

    FDA registration
    SPECTRUM VASCULAR·2 products·🇺🇸 United States

    L-Cath PICC SL

    FDA registration
    Sterigenics US LLC·2 products·🇺🇸 United States

    Cook Incorporated

    FDA registration
    Cook Incorporated·2 products·🇺🇸 United States

    Cardinal Health

    FDA registration
    Cardinal Health·2 products·🇺🇸 United States

    L-Cath™ Midline Catheters

    FDA registration
    ARGON MEDICAL DEVICES INC.·2 products·🇺🇸 United States

    Cook Incorporated

    FDA registration
    Cook Incorporated·2 products·🇺🇸 United States

    3-DAY BIOINDICATOR RELEASE PROCESS FOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TANTONE MULTI-DAY #633 TENS ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ONCE-A-DAY VERTOS TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMO PRESTIGE DAY PACK (ALLERGAN, INC.)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    3-DAY BIOINDICATOR RELEASE FOR RESPIR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology