BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    BioFlux Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SCHWERT

    FDA UDI
    A. Schweickhardt GmbH & Co. KG·E8961723110·Exchange blade for bone scraper, straigt

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100844·MCNEILL GLOBAL FIXATION RING SMALL

    TRUEPLUS SINGLE USE INSULIN SYRINGES

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code FMF·February 8, 2024

    ALP 501 RB PUMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TILITE AERO X

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SYRINGES

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code FMF·March 20, 2024

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014

    URETEX SUP URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code OTN·April 24, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 18, 2008