BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    MINIMED 508 INSULIN PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Coblation

    FDA UDI
    Smith & Nephew, Inc.·00817470001419·PERC DC (OLD)

    PROCARE

    FDA UDI
    DJO, LLC·00888912037914·ULNAR NERVE PROTECTORS 1.5 DENSITY, 36 PR/BX

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556812945·RESECTION GUIDE PIN

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 8, 2006

    ELECTRONIC HOUSE CALL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PressOn Electrode Headset

    FDA 510(k)
    FDA Class 2 ·Neurology

    INDIGO 1.0CM LASER FIBER

    FDA Adverse Event
    Death ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEX·June 22, 2006

    ISE SODIUM ELECTRODE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·March 5, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·February 8, 2011

    ADAPTA SR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·August 8, 2014

    THERASPHERE

    FDA Adverse Event
    Death ·BIOCOMPATIBLES UK LTD·Product code NAW·August 28, 2019