BEUDAMED
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    Jetox

    FDA UDI
    TAV - TECH LTD·07290014242289·

    Jetox

    FDA UDI
    TAV - TECH LTD·07290014242265·

    Jetox

    FDA UDI
    TAV - TECH LTD·07290014242029·

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·May 2, 2001

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMELRY US·Product code GDW·April 25, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 14, 2010

    CAPSURE SP NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 14, 2010

    MB & J NO BOUNCE MALLET

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HXL·September 30, 2009

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMELRY US·Product code GDW·April 25, 2014

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US·Product code GDW·April 25, 2014

    PERMANENT PACEMAKER ELECTRODE

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

    IMPELLA 5.5

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·June 9, 2025

    GUARDIAN SENSOR 3

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZP·December 10, 2021

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE MEDICAL DEVICE CENTER·Product code KNT·September 22, 2024

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 8, 2019

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code GZB·November 10, 2017

    ARGON STAINLESS STEEL GUIDE WIRE

    FDA Adverse Event
    Malfunction ·ARGON·Product code DQX·December 28, 1992

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·September 18, 2015

    TRELLIS 8 120X15

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KRA·January 7, 2015

    BD ALARIS¿ PUMP MODULE SMARTSITE¿ INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 3, 2023