BEUDAMED
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    TRANSANAL ENDOSCOPIC MICROSURGERY (TEM) COMBINATION SYSTEM AND INSTRUMENT SET, INSTRUMENT SET FOR THE TRANSANAL ENDOSCOP

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

    DTS-3000

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809315676502·RED MAIN HOSE 1ea

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040015568·Scissor Crown & Collar 4" Strt

    truFreeze

    FDA UDI
    Csa Medical, Inc.·00857068006082·16 Fr Active Venting Kit. 5 - 16 Fr Active Ven...

    Ventstar Oxylog 1000 180

    FDA UDI
    Drägerwerk AG & Co. KGaA·04048675252313·

    eWave 6-Lead EKG

    FDA UDI
    Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2520001800·Curved Ti Rod, 180mm

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2530001800·Curved Anti-Rotation Ti Rod, 180mm

    Lattus

    FDA UDI
    Seaspine Orthopedics Corporation·10889981307653·Posterior Blade, SS, 180mm

    Lattus

    FDA UDI
    Seaspine Orthopedics Corporation·10889981307752·Cephalad/Caudal 180mm Blade, AL

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·December 3, 2024

    Matrix Wearable

    FDA UDI
    GLOBAL INSTRUMENTATION, LLC·00815187020556·M5 Recorder

    ASNIS III CANNULATED SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAMLOG ROOTFORM IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 18, 2021

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·March 8, 2013

    RENAISSANCE 26 STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·February 3, 2011

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES, INC.·Product code MIH·February 18, 2008

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·October 25, 2019

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 25, 2019