Duns Number:530120146
Device Description: The Monitor is intended to be used for monitoring, displaying, reviewing, storing and alar The Monitor is intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters including ECG(3-lead, 5-lead, 12-lead selectable), arrhythmia detection, ST segment analysis, HR, Respiration Rate(RESP), TEMP, Pulse Oxygen Saturation(BLT-SpO2), PR, NIBP, IBP, CO2, Anesthetic Gas(AG), Impedance Cardiograph(ICG), CSI, BIS, SpHb, SpCO, and SpMet
Catalog Number
-
Brand Name
Patient Monitor
Version/Model Number
Q5
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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"
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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
K131898
Product Code
MWI
Product Code Name
Monitor,Physiological,Patient(Without Arrhythmia Detection Or Alarms)
Public Device Record Key
663fb97d-8567-4e5c-9e88-74d4fe1efd8c
Public Version Date
November 10, 2021
Public Version Number
6
DI Record Publish Date
September 22, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 35 |