BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PERM-A-CATH

    MDR report key: 22261 · Received May 15, 1995

    Report

    Report Number
    22261
    Event Type
    Injury
    Date Received
    May 15, 1995
    Date of Event
    April 28, 1995
    Report Date
    May 15, 1995
    Manufacturer
    UNKNOWN
    Product Code
    FIQ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    LA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CATHETER WAS REMOVED SINCE IT WASN'T WORKING WELL. PHYSICIAN EXPECTED BETTER OPERATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PERM-A-CATH Implant PERM-A-CATH FIQ UNKNOWN NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Other| R