BEUDAMED
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    MODEL 556-01 CRYOEXTRACTOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199243·AK3 PS Notch Reamer Guide Size 2

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065630·INTRAORAL ELASTICS 2,5 oz 1/8" brown

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790102000·discovery® Bracket, + 8° Torque, + 9° Angulatio...

    SurgyCut

    FDA UDI
    U.S. SURGITECH INC.·00810014632063·SurgyCut L - Hook with Handle Electrode, 5mm/45cm

    SurgyCut

    FDA UDI
    U.S. SURGITECH INC.·00810014631042·SurgyCut L - Hook with Handle Electrode, 5mm/35cm

    DyeVert™ Plus Contrast Reduction System, DyeTect™ Contrast Monitoring System, DyeVert™ Plus EZ Contrast Reduction System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NIAGARA, NIAGARA SLIM-CATH, AND BREVIA SHORT-TERM CURVED EXTENSION HEMODIALYSIS CATHETERS

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

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·May 5, 2014

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 15, 2012

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·August 5, 2010

    BD ALARIS¿ EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022