BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PEERBRIDGE COR

    MDR report key: 24215446 · Received January 29, 2026

    Report

    Report Number
    3014111150-2026-00001
    Event Type
    Injury
    Date Received
    January 29, 2026
    Date of Event
    January 1, 2026
    Report Date
    January 29, 2026
    Manufacturer
    PEERBRIDGE HEALTH, INC.
    Product Code
    DRX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT CALLED IN AND REPORTED SEVERE ITCHING AND PAIN UNDER ADHESIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    269591 PEERBRIDGE COR ADHESIVE ELECTRODE DRX PEERBRIDGE HEALTH, INC. PRT-20141E

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other