The WIZ-A101 is a compact, portable diagnostic instrument designed for clinical use that performs rapid fluorescence immunoassay testing using single-use cassettes to deliver reliable results at the point of care.
It uses advanced fluorescence immunoassay (FIA) technology to detect target analytes with high sensitivity and specificity.
Compatible sample types depend on the specific assay cassette; commonly supported matrices include whole blood (fingerstick), serum, plasma, urine or saliva. Refer to the cassette/test insert for approved sample types.
The analyzer delivers results within minutes. Exact turnaround time varies by assay — typical runtimes range from about 5 to 30 minutes depending on the test.
The WIZ-A101 processes one cassette at a time. Hourly throughput depends on assay runtime (for example, a 10-minute assay could enable up to ~6 tests per hour performed sequentially).
The system uses single-use disposable test cassettes specific to each assay. Additional consumables may include pipettes, sample transfer devices, and control materials. Use only manufacturer-approved consumables for validated performance.
The unit is designed to be compact and lightweight for clinic and mobile use. Power options and battery availability depend on the configured model — consult the product specifications or contact sales for details about AC vs. battery operation and run time.
Data handling and connectivity options (such as USB, Ethernet, Wi‑Fi or serial output) depend on model and configuration. Contact the manufacturer for available interfaces and data export formats.
The product is ISO certified, indicating compliance with international quality management standards. Local regulatory approvals (CE, FDA clearance/510(k), etc.) vary by market and assay — check with the manufacturer for specific regulatory status in your region.
The WIZ-A101 is supplied with a 24-month warranty. OEM and ODM customization and customizable service plans are available; technical support and maintenance packages can be arranged through the manufacturer or authorized distributor.
The system is designed for ease of use with streamlined cassette workflows, but operator training is recommended. The manufacturer typically provides user manuals and can provide on-site or remote training and technical support.
Routine QC and calibration procedures depend on the assays in use. Users should run manufacturer-recommended control materials at the frequency specified in the assay inserts and follow the operator manual for calibration and verification steps.
Storage conditions and shelf life vary by assay and are printed on the cassette packaging and package insert. Follow the labeled storage temperature and expiration date to ensure reliable results.
Regular basic cleaning and inspection should be performed per the user manual. Preventive maintenance intervals and any required service by authorized technicians are described in the service documentation. Use only recommended cleaning agents and procedures.
Contact the manufacturer's sales team or an authorized distributor to discuss ordering, pricing, lead times and available OEM/ODM customization options. Provide your clinical requirements so they can propose appropriate assay and hardware configurations.
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