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1.2 - i-STAT Alinity Instrument

Intended Use

The i‑STAT Alinity instrument is intended for use in the in vitro quancaon of various analytes in whole

blood or plasma in point of care or clinical laboratory sengs.

Instrument and cartridges should be used by healthcare professionals trained and cered to use the

system and should be used according to the facility's policies and procedures.

Note: Consult the IFU/CTI for details on specic sample types for the cartridge.

For in vitro diagnosc use.

Note: Not all cartridges are available in all regions. Check with your local representave

for availability in specic markets.

Note: To congure the instrument's prinng method, refer to the i-STAT Alinity Printer

Principles of Operaon

Verify the instrument for cartridge tesng

Note: Vericaon is only required once per cartridge type per instrument.

Prior to using an instrument requiring a specic cartridge type, verify the instrument supports the

cartridge:

1. Iniate a liquid quality control test per the instrucons in Liquid Quality Controls of the System

Operaons Manual.

2. Ensure the instrument can successfully scan the cartridge pouch barcode.

3. If the cartridge is not recognized, contact your local representave.

i-STAT Alinity — System Operaons Manual Art: 745527-01 Rev. N Rev. Date: 13-Oct-2022

Abbott i-STAT Alinity User Manual

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