BEUDAMED
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    Ultra PC% Cabinet Mount Package H, No Shut-offs

    FDA UDI
    ACCUTRON, INC.·00813830022698·

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·April 10, 2012

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JTC·September 16, 2003

    MICROLAB AT PLUS 2

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·April 30, 2004

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JTC·December 6, 2002

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JTC·November 27, 2002

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JTC·December 20, 2002

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Other ·HAMILTON BONADUZ·Product code JTC·March 12, 1997

    PRISMA CONTROL UNIT

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·December 20, 2006

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Other ·HAMILTON BONADUZ AG·Product code JTC·December 11, 1997

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRA·July 28, 2025

    ABBOTT AMBULATORY INFUSION-AIM PLUS PUMP

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FRN·December 10, 2001

    AMISTEM H, HA COATED STEM SIZE 2 LAT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 1, 2017

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    CADD® CADD-LEGACY® DUODOPA PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL, ASD, INC.·Product code LZH·September 5, 2018

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code LZG·August 25, 2016

    CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LZH·April 12, 2021

    FREESTYLE FREEDOM LITE

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC., USA·Product code LFR·December 22, 2008

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·December 4, 2009

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code KPF·October 27, 2006