Supply Fully Auto 5 Part Hematology Analyzer Medical Blood Test CBC Analyzer Clinical Analytical Instruments

It is a fully automatic clinical hematology analyzer that performs 5-part white blood cell differentials and routine CBC (complete blood count) testing for hospitals, clinics and laboratories, with an LCD display showing histograms.

It provides a 5-part WBC differential (neutrophils, lymphocytes, monocytes, eosinophils, basophils) and routine CBC parameters such as RBC, HGB, HCT and platelet counts. For a full parameter list please confirm with the manufacturer/spec sheet.

This analyzer is designed for anticoagulated whole blood samples. Confirm the recommended anticoagulant (typically K2/K3 EDTA) and exact sample volume in the user manual or with the supplier.

Processing time and throughput depend on sample handling and configuration. The exact time-per-sample and samples-per-hour specification are provided by the manufacturer—please contact the supplier or consult the technical documentation for precise figures.

The analyzer requires manufacturer-recommended reagents, diluents, and quality control materials. Use only approved consumables and follow reagent storage/handling guidelines. Contact the supplier for part numbers and ordering information.

Perform routine internal and external quality control using certified control materials, and follow the instrument calibration procedures in the user manual. The supplier can provide recommended QC frequency and calibration services.

Regular maintenance typically includes daily/weekly cleaning, reagent replacement, and periodic preventive maintenance per the manual. Schedule manufacturer-recommended servicing and keep maintenance logs. Online technical support is available for troubleshooting.

The unit features an LCD with histograms for results review. Connectivity (USB, LAN, LIS/HIS integration) may be available depending on model/configuration—confirm supported interfaces with the supplier.

The listed single package size is 130 x 130 x 130 cm and the single gross weight is 130.000 kg. Because of this weight and size, transportation and installation may require multiple people or special handling equipment.

The product is described as Instrument Classification: Class II. Regulatory approvals and certifications (CE, FDA clearance, ISO) can vary by market—verify applicable certifications and local registration requirements with the manufacturer or supplier before clinical use.

Suppliers commonly offer on-site installation and user training or remote training sessions. Contact the vendor to arrange installation, validation, and operator training packages.

Online technical support is listed as available. Warranty terms (duration and coverage) vary by seller—request the warranty policy, service-level details, and options for extended support from the supplier.

Follow troubleshooting steps in the user manual: check reagents and sample quality, restart the instrument if instructed, ensure maintenance tasks are up to date, and contact technical support if the issue persists. Keep error codes and conditions handy when contacting support.

It is suitable for hospitals, clinics and laboratories. Due to packaging weight and installation needs, assess space, power, and staffing requirements before deploying in small or point-of-care settings.

Contact the manufacturer or authorized distributor for pricing, lead time, and shipping arrangements. Provide site details so the vendor can advise on delivery logistics, installation requirements and any required site preparation.