Vios Monitoring System Bedside Monitor - The Vios Monitoring System (VMS) Bedside Monitor - MURATA VIOS PRIVATE LIMITED

Duns Number:874148340

Device Description: The Vios Monitoring System (VMS) Bedside Monitor is intended for use by medically qualifie The Vios Monitoring System (VMS) Bedside Monitor is intended for use by medically qualified personnel for physiological vital signs monitoring of adult (18+) patients in healthcare facilities. It is indicated for use in monitoring of 7-Lead ECG, heart rate, respiratory rate, pulse rate, functional oxygen saturation of arterial hemoglobin, non-invasive blood pressure, and patient posture and activity. VMS allows for the input of body temperature and can display data from peripheral devices. VMS can generate alerts when rate-based cardiac arrhythmias are detected and when physiological vital signs fall outside of selected parameters.The VMS Bedside Monitor is intended to be used by Vios-trained clinical professionals who also have a working knowledge of medical procedures, practices, and terminology, as required for monitoring patients.

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More Product Details

Catalog Number

BSM2050

Brand Name

Vios Monitoring System Bedside Monitor

Version/Model Number

BSM2050 Software

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K172586

Product Code Details

Product Code

DPZ

Product Code Name

Oximeter, Ear

Device Record Status

Public Device Record Key

c35163a8-e679-418a-a3c3-44fdb1ab96bf

Public Version Date

November 10, 2021

Public Version Number

3

DI Record Publish Date

May 01, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MURATA VIOS PRIVATE LIMITED" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3
2 A medical device with a moderate to high risk that requires special controls. 2