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

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    ULTRAFLOTATION BED

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Battery module

    FDA UDI
    Maquet Critical Care AB·07325710003909·

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65858826071·Doc Yang Herina Pack

    MRI-PLAQUE VIEW, VERSION 1.1.2003

    FDA 510(k)
    FDA Class 2 ·Radiology

    TERPERATUR SENSING DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·February 7, 2017

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·February 7, 2017

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·February 7, 2017

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2014

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 26, 2010

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·December 20, 2012