BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    TransFix/EDTA Vacuum Blood Collection Tubes

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HALO90 COAGULATION CATHETER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PAINSMART

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - TOONGABBIE·Product code KPE·July 14, 2011

    UTERINE ARTERY EMBOLIZATION

    FDA Adverse Event
    Injury ·Product code NAJ·September 15, 2008

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·January 9, 2024

    RHYTHMIA HDX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

    EQUINOXE PRESERVE STEM 12MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·May 29, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

    EQUINOXE REVERSE 46MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 2, 2024