BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TERUMO MEDICAL CORP ANGIO-SEAL

    MDR report key: 24686632 · Received March 25, 2026

    Report

    Report Number
    MW5185761
    Event Type
    Injury
    Date Received
    March 25, 2026
    Report Date
    March 17, 2026
    Manufacturer
    TERUMO MEDICAL CORP.
    Product Code
    MGB
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    POST SURGICAL BLEEDING AT THE SITE WHERE THE TERUMO ANGIO-SEAL WAS USED IN MULTIPLE PATIENTS WITH TIMEFRAMES FROM 7 - 24 HOURS POST PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    744613 TERUMO MEDICAL CORP ANGIO-SEAL DEVICE, HEMOSTASIS, VASCULAR MGB TERUMO MEDICAL CORP. 1454011

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown