BEUDAMED
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    DS Z-SERIES FOLDING ROLLATOR

    FDA Adverse Event
    Injury ·MAXHEALTH CORP.·Product code ITJ·September 16, 2016

    CARDINAL HEALTH BATTERY

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code DSZ·March 23, 2012

    INTERMEDICS, INC.

    FDA Adverse Event
    Injury ·INTERMEDICS, INC.·Product code DSZ·January 11, 1995

    PACEMAKER

    FDA Adverse Event
    CARDIAC PACEMAKER INC.·Product code DSZ·December 30, 1994

    ITRELL GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DSZ·June 17, 1993

    MEDTRONIC

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code DSZ·April 28, 1993

    MEDTRONICS

    FDA Adverse Event
    Injury ·MEDTRONIC INC.·Product code DSZ·May 5, 2004

    REFLEX DDD

    FDA Adverse Event
    TELECTRONICS·Product code DSZ·February 19, 1992

    HIGHRATE PACEMAKER BATTERY

    FDA Adverse Event
    MEDTRONIC, INC.·Product code DSZ·January 31, 1997

    PROTOSE DR BIOTRONIK BATTERY

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code DSZ·November 12, 2004

    N/A

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code DSZ·November 20, 1992

    CORDIS PACES

    FDA Adverse Event
    Malfunction ·CORDIS·Product code DSZ·December 29, 1992

    N/I

    FDA Adverse Event
    Malfunction ·SIEMENS PACE SETTER SYSTEMS, INC.·Product code DSZ·December 29, 1992

    MEDTRONIC DUAL CHAMBER PACEMAKER

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DSZ·August 16, 1993

    VERSIPOWER BATTERY MODULE

    FDA Adverse Event
    Other ·ZIMMER-HALL SURGICAL·Product code DSZ·June 13, 1994

    Companion External Battery, Part Number: 293001-001 The Companion External Battery is a component of the Companion 2 Driver System and the Companion Driver System. Both Driver Systems, with the temporary Total Artificial Heart (TAH-t) are indicated for use as a bridge to transplantation in cardiac transplant-eligible candidates at risk of imminent death from biventricular failure.

    FDA Recall
    Terminated ·SynCardia Systems Inc.·Product code DSZ·December 5, 2012

    Hemashield Finesse Ultra-thin Knitted Cardiovascular Patch.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DSZ·May 24, 2010

    Pacemaker Battery

    FDA classification
    FDA Class 3 ·Pacemaker Battery

    D.Z. MEDICALE S.R.L.

    Manufacturer
    🇮🇹 Italy·13 Basic UDI-DIs·13 Devices·ICIM S.P.A., ICIM S.P.A., and ICIM S.P.A.

    Junquera y Diz S.L.

    Manufacturer
    🇪🇸 Spain·4 Basic UDI-DIs·10 Devices