BEUDAMED
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    RETROGRADE KNIFE

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    DSQ Alert Candida auris Probe Mix ASR

    FDA UDI
    Elitechgroup Mdx LLC·03661540952548·DSQ Alert™ Candida auris Probe Mix ASR is an an...

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867042520·3 HOLE DBL COMP PLATE, 30MM

    IMPOAID

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    pjur WOMAN Nude pjur med SENSITIVE glide

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    OXF TWIN-PEG CMNTD FEM MD PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 22, 2020

    OXF UNI TIB TRAY SZ D LM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 22, 2020

    INTERSTIM NEUROSTIMULATOR, UNKNOWN

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·May 8, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 22, 2012

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·August 4, 2010

    UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·July 30, 2015

    OXF ANAT BRG LT MD SIZE 5 PMA

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code NRA·January 22, 2020

    OXF ANAT BRG LT MD SIZE 5 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·March 30, 2020

    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021

    ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·February 9, 2022