BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    TEN20 CONDUCTIVE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ARTERIAL HEALTH PACKAGE (AHP) SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    Blue Non-Sterile Powder Free Nitrile Examination Gloves, Tested for Use with Low Dermatitis and Fentanyl Permeation Resistance Claim

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MAYFIELD TRIAD SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA-OHIO, INC·Product code HBL·October 19, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 7, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·December 21, 2012