BEUDAMED
    2,944 results · 21ms · Sources: EU EUDAMED, US FDA

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    External Moisturizing Gel

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741718550·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674171855060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587C17185540·17mm H x 18mm W x 55mm L x 4 degree XLIF Corona...

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657015189·Grasping Forceps, 3.4mm tube diameter

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111227516·PROVIDENCE HOSP FCP STR 5 1/2"

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180533994·55mm A-ARM BLADE, NARROW

    HY-BOND RESIGLASS

    FDA 510(k)
    FDA Class 2 ·Dental

    PROFAST+ ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2014

    6000 CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 23, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 14, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 6, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 5, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·September 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 24, 2021