BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CLINIPAD IODOPHOR PVP, POVIDONE IODINE USP

    MDR report key: 275224 · Received April 26, 2000

    Report

    Report Number
    1036962-2000-00009
    Event Type
    Injury
    Date Received
    April 26, 2000
    Date of Event
    March 7, 2000
    Report Date
    April 18, 2000
    Manufacturer
    THE CLINIPAD CORP.
    Product Code
    LKB
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CLINIPAD IODOPHOR PVP, POVIDONE IODINE USP POVIDONE IODINE PREP PAD LKB THE CLINIPAD CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1