It is an automated clinical hematology analyzer designed to perform complete blood counts (CBC) with 3-part or 5-part differential options. The unit is intended for professional use in clinical and veterinary laboratories and delivers rapid, routine hematology parameters with a clear user display and online technical support.
A 3-part differential classifies white blood cells into three groups (typically neutrophils, lymphocytes and mid cells), while a 5-part differential provides a more detailed breakdown into five types (neutrophils, lymphocytes, monocytes, eosinophils and basophils). The choice depends on the level of diagnostic detail required.
Yes — the product description states suitability for both human and veterinary applications. Operators should follow local regulatory requirements for human diagnostics and validate performance for each animal species before clinical use.
According to the description, the analyzer complies with CE and ISO certification standards and is classified as a Class II instrument. Always verify current certification documents with the supplier.
The analyzer is designed for blood samples used in routine CBC testing. Most hematology analyzers use EDTA-anticoagulated whole blood; check the user manual or supplier documentation for approved sample types, volumes and handling instructions.
The analyzer is described as delivering accurate and reliable results and conforms to CE/ISO standards. As with any clinical instrument, accuracy depends on following calibration, quality control procedures and using approved reagents and consumables.
The analyzer requires reagents, calibrators and quality control materials typical for CBC testing. Exact reagent part numbers and compatible controls should be provided by the manufacturer or supplier; confirm whether OEM or validated third‑party consumables are recommended.
Online technical support is available according to the description. For onsite training, installation assistance or extended service agreements, contact the supplier to confirm available options.
Routine maintenance (daily/weekly cleaning, reagent replacement, and periodic calibration) and running quality controls are standard practice. Specific maintenance schedules and calibration procedures are provided in the user manual; contact technical support for service guidance.
The single package dimensions are listed as 50 x 50 x 50 cm with a gross weight of 16.0 kg. Actual instrument dimensions and net weight should be confirmed with the vendor.
The description lists 'OEM' and 'Accept OEM,' indicating that original equipment manufacturer (OEM) or private‑labeling options may be available. Discuss customization, branding or OEM requirements with the supplier.
The product description mentions a clear display but does not list specific connectivity options. Many modern analyzers offer interfaces such as USB, LAN or serial connections and LIS protocols. Check the model's technical specifications or ask the supplier for available data export/integration options.
Warranty and service terms are not specified in the brief description. Ask the seller for details about warranty length, what is covered, available service contracts and response times for repair or replacement.
The description notes applicability to emergency medical services for quick blood assessments. Whether it is suitable for point‑of‑care (POC) deployment depends on factors such as portability, power requirements and regulatory approvals for POC use; confirm these details with the vendor.
Contact the manufacturer or authorized distributor (brand listed as Antonmed in the description) to place an order. Ask about delivery, installation, validation, operator training and online technical support options before purchase.
Discover our latest orders