BEUDAMED
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    MODOFICATION TO AFFFINITY 38 MICRO ARTERIAL BLOOD FILTER WITH CARMEDA BIOACTIVE SURFACE, MODELS CB351/CB352

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810003791·LUKS FINGER PLUGGER 25MM

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040094669·Finger spreaders 25 mm B

    NA

    FDA UDI
    TORNIER, INC.·00846832088461·Fukuda

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040179468·Diamond Discs

    Eclipse Pro

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522128721·ECLIPSE PRO,CABLE,PX,4 SNAP,SHORT

    NUZONE NITRILE SURGICAL GLOVES POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M

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

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 12, 2013

    TALENT CONVERTER STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 18, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·February 15, 2008

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·September 25, 2024

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·July 13, 2023

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·May 23, 2024

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·June 7, 2024

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·November 28, 2024

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·October 31, 2023

    LEEP BALL ELECTRODE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·February 2, 2024

    HLS CANNULA + PIK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWF·November 21, 2024

    ConMed Eliminator Esophageal PET Balloon Dilator; Outer Diameter (OD) size 20mm (60 Fr), length 8cm; product code/end item #000380 and #000379 (5 pack); Single Use, Non-Sterile; distributed by ConMed Endoscopic Technologies, Billerica, MA 01821.

    FDA Recall
    Terminated ·Conmed Endoscopic Technologies, Inc.·Product code KNQ·April 16, 2007