BEUDAMED
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    HAEMOTRONIC BLOOD LINE SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867241251·Large Combination Clamp

    LEUCOPREP CELL SEPARATION TUBE

    FDA 510(k)
    FDA Class 1 ·Hematology

    THE SAXON SPERMICIDAL CONDOM W/2 YEAR EXPIRATION

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

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 7, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 27, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 16, 2018

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 7, 2015

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 16, 2014

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    STRAIGHT ATTACHMENT ARM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    LARGE COMBINATION CLAMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·April 21, 2026

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 5, 2018

    LARGE COMBINATION CLAMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·April 21, 2026

    LARGE COMBINATION CLAMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·April 21, 2026

    LARGE COMBINATION CLAMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·April 21, 2026

    5.0MM SELF DRILL SCHANZ SCREW, 200MM, SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NDK·April 22, 2026

    LARGE COMBINATION CLAMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·April 21, 2026