BEUDAMED
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    Phoenix Ultra Chain

    FDA UDI
    PHOENIX ORTHODONTICS INC·05060772895018·U CHAIN OPEN COBALT SPOOL 15 FEET

    COMET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DXO·March 27, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·July 6, 2007

    COMET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DXO·February 6, 2019

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 12, 2015

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·May 31, 2007

    GE OEC 6800 MINIVIEW

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·August 22, 2007

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·August 29, 2013

    BREVERA BREAST BIOPSY SYSTEM

    FDA Adverse Event
    Injury ·HOLOGIC, INC·Product code KNW·November 1, 2024

    IMPLANTABLE COLLAMER LENS (ICL)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·April 17, 2021

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·May 8, 2007

    SCULPTRA (POLY-L-LACTIC ACID)

    FDA Adverse Event
    SANOFIAVENTIS U.S. LLC.·Product code LMH·December 8, 2009

    GENESEARCH BREAST LYMPH NODE ASSAY

    FDA Adverse Event
    Other ·VERIDEX LLC·Product code OCB·February 14, 2008

    COMET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DXO·April 24, 2019

    BREVERA BREAST BIOPSY SYSTEM WITH CORLUMINA IMAGING TECHNOLOGY

    FDA Adverse Event
    Injury ·HOLOGIC, INC·Product code KNW·December 7, 2022

    ONCENTRA BRACHY TPS

    FDA Adverse Event
    NUCLETRON·Product code MUJ·December 23, 2014

    COLOPLAST TITAN PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·COLOPLAST MANUFACTURING US, LLC.·Product code FHW·May 22, 2025

    ONCENTRA BRACHY

    FDA Adverse Event
    Malfunction ·NUCLETRON B.V.·Product code JAQ·November 10, 2022

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 23, 2020

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·September 19, 2013