BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER

    FDA 510(k)

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA 510(k)
    FDA Class 2 ·Hematology

    XVWEB

    FDA 510(k)
    FDA Class 2 ·Radiology

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE·Product code OUR·January 24, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·December 17, 2010

    ECHELON*FLEX60 LONG ARTICULATING

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 14, 2014

    XVWEB

    FDA Adverse Event
    Injury ·PLANET DDS·Product code LLZ·March 13, 2025

    SECOND OPINION

    FDA Adverse Event
    Injury ·PEARL INC.·Product code MYN·March 13, 2025