BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Lumax

    Reg #: 1028232 · FEI: 1028232 · Expires 2025
    View on FDA
    Products
    7
    Proprietary Names
    24
    Establishment Types
    1
    Classifications
    7

    Registration Details

    Registration Name
    BIOTRONIK, INC.
    Registration Number
    1028232
    FEI Number
    1028232
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    6024 JEAN RD.
    City
    LAKE OSWEGO
    State
    OR
    ZIP
    97035
    Country
    US

    Regulatory Submissions

    PMA Number
    P050023

    Owner / Operator

    Firm Name
    BIOTRONIK, INC.
    Operator Number
    1028232
    Address
    6024 JEAN RD., --
    City
    Lake Oswego
    State
    OR
    Postal Code
    97035
    Country
    US
    Correspondent
    JON - BRUMBAUGH

    Products

    Device Name Product Code
    Pacemaker/Icd/Crt Non-Implanted Components OSR
    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D) NIK
    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode OJX
    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P) NKE
    Defibrillator, Implantable, Dual-Chamber MRM
    Implantable Cardioverter Defibrillator (Non-Crt) LWS
    Pulse Generator, Permanent, Implantable NVZ

    Proprietary Names

    Lumax Home Monitoring Iforia Ilesto DF4 Iforia DF4 Ilesto Itrevia DF4 Itrevia Iperia Inventra DF4 Inventra HF-T QP Itrevia HF-T QP Iperia DF4 Inventra Iperia HF-T QP PSW 1507.U Intica PSW 1506.U BS IS4 Ilivia Acticor family CardioMessenger Renamic ICS 3000

    Establishment Types

    Repack or Relabel Medical Device