BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    ADULT VENT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REINFORCED SILICONE TRACHEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    3-DAY RELEASE OF ETHYLENE OXIDE DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UNKNOWN EXTERNAL NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·November 15, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 28, 2014

    PROTECTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 10, 2015