I stat1 is tested with electronic quality checks using an electronic simulator to confirm analyzer performance.
I stat machine purpose.
Procedure manual for the i stat system sop 111 800 005 rev 05 21 2018 1 i.
Poor storage conditions of cartridges frozen or too warm.
Ensure cartridges were not frozen.
It simulates two levels of electrical signals that stress the analyser s cartridge signal detection function both below and above measurement ranges.
End the waiting game with the i stat handheld blood chemistry analyzer.
This portable tool helps you provide a patient centered approach allowing you to diagnose and treat in the same visit.
If test passes on the 2nd i stat analyzer call poct technologist.
Manufacturer of the i stat system a handheld blood analyser for with patient testing aimed at improving the quality cost and operational efficiency of health.
A portable handheld a cartridge with the required tests and 1 to 3 drops of blood will allow the caregiver to view.
Abbott park il 60064 usa 20 jan 2012 electronic simulator quality control regimen.
I stat electronic simulator the electronic simulator is a quality control device for the analyser s cartridge signal reading function.
Read frequently asked questions about i stat system product ordering technical troubleshooting software updates and more.
Pressure in center of the cartridge try another cartridge.
The i stat system incorporates components needed to perform blood analysis at the patient s side.
Abbott point of care inc.
For the i stat system this procedure manual is intended to be a template for the procedure manual required by clia and laboratory accreditation bodies.
The procedure manual is provided on cd rom for this purpose.
Cartridge preburst use another cartridge analyzer has detected fluid on the sensors before it should have.
An advanced easy to use blood analyzer that provides healthcare professionals with access to lab quality results in minutes for point of care testing.
This procedure manual should be customized for site specific policies and procedures.
Once every 24 hours when instrument not in use.