BEUDAMED
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    MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER

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

    Surgimedics®

    FDA UDI
    COASTAL LIFE TECHNOLOGIES, INC.·00814716020647·Smoke Evacuation Tubing

    Eclipse®

    FDA UDI
    Dentsply International Inc.·D0019050800·Clear

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867317024·LOW PROFILE CORTICAL SCW, TI, 5.0x80MM

    EZ-BEAD PHENYTOIN ENZYME IMMUNOASSAY KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NEW IOWA MOTILITY IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code NIU·May 22, 2014

    CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·January 9, 2013

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 22, 2010

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code ERL·March 31, 2015

    GENTLECATH GLIDE

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code GBM·August 30, 2022

    GENTLECATH GLIDE

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code GBM·August 30, 2022

    Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes.

    FDA Enforcement
    Class I ·Terminated·Animas Corporation·April 10, 2013