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Vios Monitoring System Central Server

FDA UDI

Class I (US FDA UDI)

by Murata Vios, Inc.

Identity

Trade Name
Vios Monitoring System Central Server FDA UDI
Generic Name
Network server FDA UDI
Device Name
The Vios Monitoring System (VMS) Central Station Monitor (CSM)/Central Server (CS) Software (SW) is indicated for use by healthcare professionals for the purpose of centralized monitoring of patient data within a healthcare facility. The Vios CSM SW and CS SW receives, stores, manages and displays patient physiological and waveform data and alarms generated by Vios proprietary patient vitals monitoring software. The VMS CS SW acts as the server relay for the VMS system. It transmits, stores, and encrypts patient demographic and vitals data between multiple Vios Bedside Monitors (BSMs) to the Vios CSM. The Vios CS SW allows for retrieval of patient demographics, vitals and alarm data and product utilization through retrieval of audit logs. The Vios CS SW allows for creation and configuration of Monitoring Units (i.e. Wards), Caregivers, Departments, Rooms, Beds, and Default Monitoring Profiles for BSMs that are in Connected Mode. FDA UDI
Model / Reference
VCS2050 Software FDA UDI
Description
The Vios Monitoring System (VMS) Central Station Monitor (CSM)/Central Server (CS) Software (SW) is indicated for use by healthcare professionals for the purpose of centralized monitoring of patient data within a healthcare facility. The Vios CSM SW and CS SW receives, stores, manages and displays patient physiological and waveform data and alarms generated by Vios proprietary patient vitals monitoring software. The VMS CS SW acts as the server relay for the VMS system. It transmits, stores, and encrypts patient demographic and vitals data between multiple Vios Bedside Monitors (BSMs) to the Vios CSM. The Vios CS SW allows for retrieval of patient demographics, vitals and alarm data and product utilization through retrieval of audit logs. The Vios CS SW allows for creation and configuration of Monitoring Units (i.e. Wards), Caregivers, Departments, Rooms, Beds, and Default Monitoring Profiles for BSMs that are in Connected Mode. FDA UDI

Identifiers

Catalog Number
VCS2050 FDA UDI
Primary DI / UDI-DI
B595VCS2050 FDA UDI
510(k) Number
K173107 FDA UDI
K232354 FDA UDI
K241728 FDA UDI
FDA Product Code
OUG FDA UDI
DXJ FDA UDI
QYW FDA UDI
DXN FDA UDI
GMDN Term
Network server FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 FDA UDI
870.2450 FDA UDI
870.1025 FDA UDI
870.1130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiac arrhythmia monitoring systemNetwork server

Vios Monitoring System Central Server by Murata Vios, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Network server.

Cleared under the same submission

K173107 also covers:

K232354 also covers:

K241728 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Murata Vios, Inc.

Sources (1)

  • FDA UDI fe3b361e-45b9-4358-b701-152095f410db 36 fields · synced May 30, 2026