BEUDAMED
    FDA Adverse Event Summary report: N

    SEA BAND

    MDR report key: 16488553 · Received March 3, 2023

    Report

    Report Number
    MW5115451
    Date Received
    March 3, 2023
    Report Date
    March 1, 2023
    Manufacturer
    SEA-BAND, LTD.
    Product Code
    MVV
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT TRIED AND FAILED MEDICATION- PATIENT STATED MEDICATION DID NOT WORK. (B)(6) HCP DID CONSENT TO FOLLOW UP; (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    705934 SEA BAND DEVICE, ACUPRESSURE MVV SEA-BAND, LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown UNISOM