BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    BUTTERFLY NON-CORING NEEDLE SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO STAXX FX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Digital Blood Pressure Monitor-Automatic Upper Arm Style

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·April 17, 2020

    ISOLINE

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code MRM·June 10, 2014

    ALTRUA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 11, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 10, 2012