BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    TEFLON CERVICAL ACCESS SET

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDOTHELIAL GROWTH MEDIUM (EGM)

    FDA 510(k)
    FDA Class 1 ·Hematology

    DRILL SLEEVE, AVN

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 8, 2022

    REALSEAL SE

    FDA Adverse Event
    Injury ·SYBRONENDO·Product code KIF·June 26, 2014

    TENDRIL ST

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

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·November 21, 2012

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020