BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Murata Vios, Inc.

    Reg #: 3015328411 · FEI: 3015328411 · Expires 2026
    View on FDA
    Products
    9
    Proprietary Names
    3
    Establishment Types
    4
    Classifications
    9

    Registration Details

    Registration Name
    Murata Vios, Inc.
    Registration Number
    3015328411
    FEI Number
    3015328411
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    700 Commerce Drive, Suite 190
    City
    Woodbury
    State
    MN
    ZIP
    55125
    Country
    US

    Regulatory Submissions

    510(k) Number
    K172586

    Owner / Operator

    Firm Name
    Murata Vios, Inc.
    Operator Number
    10059850
    Address
    700 Commerce Drive, Suite 190
    City
    Woodbury
    State
    MN
    Postal Code
    55125
    Country
    US

    Products

    Device Name Product Code
    Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) DRT
    Oximeter, Ear DPZ
    Transmitters And Receivers, Physiological Signal, Radiofrequency DRG
    Oximeter DQA
    Medical Device Data System OUG
    Display, Cathode-Ray Tube, Medical DXJ
    System, Measurement, Blood-Pressure, Non-Invasive DXN
    Detector And Alarm, Arrhythmia DSI
    Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) MHX

    Proprietary Names

    Vios Monitoring System™ Model 2050 Vios Central Station Monitor/Vios Central Server Software 2050 Vios Monitoring System

    Establishment Types

    Remanufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device Repack or Relabel Medical Device