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

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    Filters Regulation: Us FDA ×

    SiOxD Wound Matrix

    FDA 510(k)
    FDA Unclassified ·Unknown

    Graffiti

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    QUIDEL MOLECULAR RSV + HMPV ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·June 6, 2003

    IMPL TAPERED SCR-V HA 3.7 MM 3.5MM 11.5MM

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·July 27, 2020

    IMPL TAPERED SCR-V HA 3.7 MM 3.5MM 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 28, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 14, 2025

    FLOWART NEEDLE-FREE SPLIT SEPTUM VALVE

    FDA Adverse Event
    Malfunction ·ASSET MEDIKAL TASARIM SAN. TIC. A.S.·Product code FPA·July 24, 2025

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 3, 2014

    PROPAQ ENCORE

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DRT·June 28, 2013

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 24, 2011