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

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    Confirm Rx Insertable Cardiac Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROVOX ACTIVALVE (SIZE 4.5MM, 6MM, 8MM, 10MM, 12.5MM)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SYNTHETIC, POWDER-FREE NITRILE EXAMINATION

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OMNIPOD 5 POD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

    OMNIPOD 5 POD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

    OMNIPOD 5 POD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 29, 2021

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·October 22, 2014

    SENSORMEDICS

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code LSZ·July 1, 2011

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·June 27, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·September 11, 2013