BEUDAMED
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    extriCARE

    FDA UDI
    OAKWELL DISTRIBUTION, INC.·00879766005723·extriCARE large oval dressing

    IMPLANTABLE NEUROSTIMULATOR FOR SCS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·March 21, 2018

    GELFILM

    FDA Adverse Event
    Malfunction ·PFIZER, INC. (DEVICE)·Product code LMF·April 24, 2019

    GELFILM

    FDA Adverse Event
    Malfunction ·PFIZER, INC. (DEVICE)·Product code LMF·April 24, 2019

    ACCU-CHEK COMFORT CURVE STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CFR·March 8, 2006

    ASCENSIA CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·June 2, 2006

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 16, 2008

    H-TRONPLUS

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·October 21, 2005

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 18, 2017

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 8, 2018

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 14, 2022

    630G INSULIN PUMP MMT-1715K 630G BLACK MG

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 10, 2018

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·January 22, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·December 9, 2016

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·July 26, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 2, 2018

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·August 4, 2023

    GELFILM

    FDA Adverse Event
    Malfunction ·PFIZER, INC. (DEVICE)·Product code LMF·April 25, 2019

    ONE TOUCH ULTRA

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·November 23, 2005

    SPF-XL IIB IMPLANTABLE SPINAL FUSION STIMULATOR

    FDA Adverse Event
    Injury ·BIOMET SPINE - BROOMFIELD·Product code LOE·September 16, 2015