For i-STAT test cartridge information and intended use, refer to individual product pages or the cartridge information (CTI/IFU) in the i-STAT Support area.Ībbott - A Leader in Rapid Point-of-Care Diagnostics. Check with your local representative for availability in specific markets. Not all products are available in all regions. The i-STAT 1 Wireless allows medical staff to quickly perform patient-side.
#Abbott istat iqcp portable#
The i-STAT 1 Wireless portable blood analyzer combines all the features of the i-STAT 1 analyzer with the convenience of wireless transmission for even greater efficiency. GDPR Statement (last updated: May 2018) | California Transparency in Supply Chains Act | Declaration for California Compliance Law. Perform diagnostic tests at the point of care and wirelessly transmit results to your EMR or LIS. Any person depicted in such photographs is a model. Photos displayed are for illustrative purposes only. Led research and implementation of Abbott iSTAT Advanced Quality Features (AQF), ensuring better quality. Your use of this website and the information contained herein is subject to our Website Terms and Conditions and Privacy Policy: US Citizens | Non-US Citizens. Individual Quality Control Protocol (IQCP).
#Abbott istat iqcp registration#
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#Abbott istat iqcp code#
Training/Competency review of monthly event logs I-stat quality check will diplay and error code if specimen is clotted and does not make it to the sensors.©2022 Abbott. Incorrect mixing of sample, wrong specimen collected, delay in testing after collection. Training/Competency I-stat quality checks will fail and testing will be stopped if insufficient sample is added to istat. Quality check failure - retesting required. Not enough sample added to meet the fill line of the reagent cartridge. Improper sample volume added to reagent cartridge If sample is clotted, istat quality check will fail and retesting will be required. Operator fails to use correct sample required for testing.Įrroneous results reported. Questionable results should be confirmed with central laboratory. Operators should be familiar with the Abbott iSTAT Creatinine list of interfering substances. Running whole blood sample with interfering substances. I-stat had built in barcoded system that prevents use of on package expiration date Random audit of reagents, monitoring expiration of reagents. Room temperature storage used after written expiration date on package Review monthly event logs for operator repeated failures.
Delay in patuent treatment and resulting. Testing error generated, repeat testing required. Squeezing cartridge at the center, handling the cartridge by the sensors. Event logs reviewed monthly for repeat patterns of operator failure. i-Stat displays error message if specimen volume is incorrect or clotted from improper mixing. Specimen recollction - delay in results and treatmentĭemonstrated correct specimen handling and testing procedure during competency assessment. Overfilling and underfilling of cartridge.Įrroneous results reported, Istat identifies error and displayed error message. Improper mixing of specimen, using specimen when quanity of blood is not sufficient. Training, Following requirments for labelling spcimens at bedside. Incorrect addressograph used for labeling patient specimenĭelay in testing and treatment Possible re-draw Incorrect specimen type collected for testing.Ĭovered during initial training, 6 month and annual competency assessment. Audit of occurences monthly Perform tracers - directly observe patient identification. Training to positively identify patient at bedside.