BEUDAMED
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    WBR XPRESS.CARDIAC AND XPRESS3.CARDIAC INCLUDING ATTENUATION AND SCATTERING CORRECTIONS

    FDA 510(k)
    FDA Class 2 ·Radiology

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450236291·

    CRYOPLAN SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PANORAMA CENTRAL STATION

    FDA Adverse Event
    Malfunction ·MINDRAY DS SUA, INC.·Product code MHX·April 30, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 16, 2014

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 12, 2011

    HI-TORQUE BALANCE MIDDLEWEIGHT¿

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·January 6, 2026

    HI-TORQUE BALANCE MIDDLEWEIGHT¿

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·January 6, 2026

    METASUL LDH, HEAD, 56, CODE V, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 27, 2018

    METASUL LDH, HEAD, 56, CODE V, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWY·January 31, 2018

    METASUL LDH, HEAD, 40, CODE F, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·June 13, 2018

    Custom Kit, Sterile EO, Rx Only, Catalog No. K09-10573, Manufactured by Merit Medical Systems, Inc. South Jordan, Utah 84095, USA,

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code DQO·October 25, 2010

    Custom Kit, Sterile EO, Rx Only, Catalog No. K09-10573, Revision A, Merit Medical Systems, Inc. South Jordan, Utah 84095, USA,

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code DQO·October 25, 2010

    THORATEC® HEARTMATE 3¿ SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·July 2, 2024

    METASUL LDH, HEAD, 44, CODE J, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KXA·October 24, 2017

    METASUL HEAD 28MM L 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·August 7, 2018

    METASUL HEAD 28MM L 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·August 3, 2018

    METASUL, HEAD, M, 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·March 12, 2018

    METASUL LDH, HEAD, 44, CODE J, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 22, 2018