BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASER-STAR CATHETER

    MDR report key: 252543 · Received December 1, 1999

    Report

    Report Number
    2020638-1999-00027
    Event Type
    Injury
    Date Received
    December 1, 1999
    Date of Event
    November 1, 1999
    Report Date
    November 2, 1999
    Manufacturer
    CORDIS WEBSTER, INC.
    Product Code
    DRF
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT SUFFERED CARDIAC ARREST POST-PROCEDURE, REQUIRING INTUBATION, INTRA-AORTIC BALLOON PUMP COUNTER-PULSATION, LEFT MAIN CORONARY ARTERY STENTING, AND LEFT ANTERIOR DESCENDING ARTERY STENTING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASER-STAR CATHETER THERAPEUTIC CATHETER DRF CORDIS WEBSTER, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Life Threatening| R 4. ANGIOGRAPHY CATH.| 3. REF-STAR,| 1. NAVISTAR,| 2. LASERSTAR,