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CoaguChek Pro II Wireless INR and PT Meter
Code: MD10474
Roche CoaguChek Pro II System
The Roche CoaguChek Pro II system is a point-of-care meter for prothrombin time (PT) and INR determination by healthcare professionals. The device is designed for use in GP practices, minor injury units, and community clinical settings where rapid coagulation assessment is required.
The meter features built-in Wi-Fi connectivity for wireless transmission of results and an integrated 1D and 2D barcode scanner for operator and patient identification. The system uses CoaguChek test strips and provides INR results for patients on anticoagulation therapy or requiring coagulation status assessment.
The device is compatible with existing CoaguChek workflows and features an intuitive user interface. The wireless functionality enables immediate availability of results without requiring manual docking or data transfer.
Product Features
- Point-of-care PT/INR testing for healthcare professionals
- Built-in Wi-Fi for wireless result transmission
- Integrated 1D and 2D barcode scanner for operator and patient IDs
- Intuitive user interface
- Compatible with CoaguChek test strips
- Suitable for anticoagulation monitoring and coagulation assessment
- No docking required for data transmission
Frequently Asked Questions
What is CoaguChek used for?
CoaguChek systems are point of care coagulometers used for the quantitative determination of Prothrombin Time (PT), reported as the International Normalised Ratio (INR).
They are used to monitor patients receiving Vitamin K Antagonist therapy, including Warfarin. INR monitoring supports anticoagulation management in conditions such as atrial fibrillation, deep vein thrombosis and in patients with mechanical heart valves.
Use should align with local anticoagulation protocols, manufacturer instructions and point of care testing governance frameworks.
How is CoaguChek used for INR monitoring?
CoaguChek meters use a capillary blood sample of approximately 8 µL to determine INR at the point of care.
Testing involves inserting the appropriate code chip and test strip, allowing the meter to complete its internal checks, and applying a fresh capillary blood sample to the test strip within the timeframe specified in the manufacturer’s instructions. The system uses an electrochemical method to detect clot formation and displays the INR result in approximately one minute.
Operation should follow the manufacturer’s instructions for use, including quality control procedures, operator training requirements and local point of care testing policies.