BEUDAMED
    1,344 results · 31ms · Sources: EU EUDAMED, US FDA

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    VITATRON M

    FDA 510(k)

    VITATRON INSERT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PACEMAKERS, VITATRON'S

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    VITATRON 88

    FDA 510(k)
    FDA Class 2 ·Neurology

    PACEMAKERS, VITATRONS (SERIES 2000)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    PACEMAKERS, VITATRONS (SERIES 3000)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 11, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 7, 2014

    CARELINK PROGRAM W/TELEMETRY C

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·August 11, 2011

    DIAMOND II DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC., CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 12, 2000

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·April 10, 2015

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 14, 2012

    DA+ C SERIES SR

    FDA Adverse Event
    Death ·VITATRON MEDICAL B.V.·Product code DXY·January 18, 2012

    VITATRON LEAD

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code DTB·August 12, 2023

    SPECTRANETICS LASER SHEATH II

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code MFA·June 15, 2012

    HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·June 11, 2012

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·April 12, 2012

    KORA

    FDA Adverse Event
    Malfunction ·MICROPORT CRM S.R.L.·Product code LWP·March 15, 2023

    PERMANENT PACEMAKER ELECTRODE

    FDA Adverse Event
    Malfunction ·VITATRON·Product code DTB·August 12, 2023