BEUDAMED
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    JetPeel

    FDA UDI
    TAV - TECH LTD·07290014242357·

    MIAMI J COLLAR

    FDA Adverse Event
    Injury ·OSSUR·Product code IQK·February 25, 2016

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 15, 2014

    MICROSTAAR INJECTOR

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code KYB·March 23, 2006

    MICROSTAAR INJECTOR

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code KYB·March 23, 2006

    CAPSURE SENSE LEAD MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·January 30, 2020

    ACCUSTICK? II

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code DYB·October 14, 2014

    LRG TAP PRI MOD NCK 0DEG 30MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code LZO·September 14, 2012

    INSYNC ICD

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·October 8, 2010

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 10, 2015

    TAQPATH COVID-19 COMBO KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP (THERMO FISHER SCIENTIFIC)·Product code QJR·July 20, 2021

    TAQPATH COVID-19 COMBO KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP (THERMO FISHER SCIENTIFIC)·Product code QJR·July 9, 2021

    LEAD

    FDA Adverse Event
    Malfunction ·BIOTRONIK·Product code NVY·August 12, 2023

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE MEDICAL DEVICE CENTER·Product code KNT·June 9, 2025

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

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·June 28, 2018

    PWRD ECH FLEX 60MM 44CM SHAFT

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 7, 2014

    QUANTUM HR

    FDA Adverse Event
    Injury ·LUMENIS (ISREAL)·Product code GEX·September 6, 2005

    TIGHTROPE ® II BTB WITH DEPLOYING SUTURE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·May 14, 2024

    MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    DATASCOPE CORP.·Product code LDD·May 31, 1994

    ABBVIE PEG

    FDA Adverse Event
    Injury ·ABBVIE MEDICAL DEVICE CENTRE·Product code KNT·February 8, 2018