BEUDAMED
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    AQUASENS FLUID MONITORING SYSTEM

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

    Audit MicroControls Control FD Assayed Chemistry, Level 2

    FDA UDI
    AALTO SCIENTIFIC·B085K0312100·

    Tiche PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481477078·

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0132130·Trial, TLIF, 27L OB CRV 7Deg, 13mm

    MODIFICATION TO SYNCHRON LX 20 CLINICAL CHEMISTRY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40, -50, & -60

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SCP PANEL CENTRIFUGE JMS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·April 2, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·March 16, 2011

    PUMP MMT-722NAB PRDGM INS V2.2 BL EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·April 17, 2008

    SYNCHRON LX 20 PRO CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 8, 2011

    SCP PANEL CENTRIFUGE JMS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·March 14, 2014

    SCP CONTROL PANEL

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

    CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWA·January 19, 2018

    CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·January 5, 2022

    STOCKERT JMS CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

    MONOPLUS VIOLET 0 (3,5) 90CM HR37S(M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.U.·Product code NEW·December 14, 2021

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 2, 2019

    MONOPLUS VIOLET 4/0 (1.5) 70CM HR17 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 23, 2019

    STOCKERT CENTRIFUGAL PUMP (SCP) SYSTEM

    FDA Adverse Event
    Injury ·SORIN GROUP DEUTSCHLAND·Product code DWA·May 7, 2010