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

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    Kaplan-Simpson InfusaSleeve II Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    "2.0" SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036075941·

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 10, 2012

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·December 12, 2012

    MODIFICATION TO: STRYKER SPINE OASYS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Stretta Catheter

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 29, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 29, 2015

    INSYNC SENTRY

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·February 9, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 23, 2014

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 7, 2011

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 28, 2014

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·December 11, 2014