What is FDA product code OUG?

A medical device data system (mdds) is a device that is intended to provide one or more of the following uses, without controlling or altering the functions or parameters of any connected medical devices: (i) the electronic transfer of medical device data; (ii) the electronic storage of medical device data; (iii) the electronic conversion of medical device data from one format to another format in accordance with a preset specification; or (iv) the electronic display of medical device data. (2) An MDDS may include software, electronic or electrical hardware such as a physical communications medium (including wireless hardware), modems, interfaces, and a communications protocol. This identification does not include devices intended to be used in connection with active patient monitoring.

General Hospital › MiscellaneousMedical Device Data System

Vios Monitoring System Central Server

Name: Vios Monitoring System Central Server
Brand: Vios Monitoring System Central Server

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…

Registry build 21.09.26

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.

11manufacturers in China registered for this device type

1catalogue number

Who Else Makes It

Concentrated in Guangdong (4), Shanghai (3), Jiangsu (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OUG
Manufacturer	City	Province	Registered as	Device types
Edan Instruments, Inc.	Shenzhen	Guangdong	Contract manufacturer	56
Jabil Circuit (Shanghai) Ltd.	Shanghai	Shanghai	Contract manufacturer	31
Dongguan BAO Kang Dian ZI KE JI Limited	Dongguan	Guangdong	Contract manufacturer	24
Primecare Medical (Suzhou) Co., Ltd.	Changshu	Jiangsu	Contract manufacturer	20
Shenzhen Insighters Medical Technology Co., Ltd.	Shenzhen	Guangdong	Contract manufacturer	10
Changshu Rozer Sterilization Technology Co., Ltd.	Changshu	Jiangsu	Contract manufacturer	43
Hangzhou Primecare Medical Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	29
Shanghai Mediworks Precision Instruments Co., Ltd.	Shanghai	Shanghai	Contract manufacturer	13
Zhejiang Yigao Medical Technology Co., Ltd.	Hangzhou	Zhejiang	Manufacturer	7
Resvent Medical Technology Co., Ltd.	Shenzhen	Guangdong	Contract manufacturer	6
Shanghai Draeger Medical Instrument Co., Ltd.	Shanghai	Shanghai	Contract manufacturer	4

Record

Regulatory record for Vios Monitoring System Central Server
Listed by	Murata Vios, Private Limited, India
FDA product code	OUG
Device type	Medical Device Data System
Device class	Class 1
Regulation	21 CFR 880.6310
Establishment	Remanufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k)	K173107
Record published	2020-05-01
Record revised	2025-03-24 (version 5)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Label carries	lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Vios Monitoring System Central Server
Catalogue number	Size	Status
VCS2050 Software		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Responder	Rauland-Borg Corporation	170
Medical Device Data System	Pentax of America, Inc.	72
DreamStation	Respironics Inc.	55
Endopro IQ	Pentax of America, Inc.	49
MonitAir	Monitair, LLC	22
Medical Device Data System	Medtronic, Inc.	20
DreamMapper	Respironics Inc.	16
Arthrex®	Arthrex, Inc.	14
Visionflex	Visionflex PTY Limited	11
Intesys Clinical Suite	Spacelabs Healthcare (Washington), Inc	11
myoncare	Oncare GmbH	9
MicroScan	Beckman Coulter, Inc.	9

Showing 12 of 281. All products under Medical Device Data System

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.