Dirui H-100 Automated Urine Analyzer

The H-100 can measure urobilinogen, bilirubin, ketone, creatinine, microalbumin and blood. Other configurations of the H-100 platform may support expanded parameter panels (for example 11 or 13 parameter kits) — check the product configuration offered by your supplier.

The analyzer operates at four precise wavelengths: 525 nm, 572 nm, 610 nm and 660 nm to ensure accurate spectrophotometric readings across its assays.

Yes. The H-100 is CE marked and ISO certified and is classified as a Class II (Class IIA) medical instrument, meeting international standards for clinical use.

The device is designed for use in hospitals, clinical laboratories and other clinical settings requiring automated urine analysis.

The H-100 is intended for human urine samples. Follow local biosafety guidelines and the user manual for correct sample handling and preparation.

The H-100 comes with a 1-year warranty. After‑sale services include repair and replacement options. For details on coverage, service response times and local support, contact the authorized distributor or Dirui representative in your region.

Yes. Like all clinical analyzers, the H-100 requires routine maintenance and periodic calibration to ensure accuracy. Refer to the operator manual for recommended maintenance schedules, calibration procedures and quality control protocols.

Consumables (such as reagent strips, controls and any platform-specific items) and spare parts should be sourced from Dirui or authorized distributors to ensure compatibility. Contact your supplier for part numbers and ordering information.

Connectivity options depend on the specific configuration and accessories. Some H-100 units may offer data export or interfacing capabilities. Confirm available communication ports and LIS compatibility with your supplier or by consulting the product documentation.

Specific installation site and power specifications are provided in the user manual and may vary by region/version. Contact the vendor for the exact electrical requirements, space, ambient conditions and installation services.

Training and user orientation are commonly offered by Dirui or authorized distributors as part of installation or service packages. Verify training availability and scope with your supplier.

The H-100 uses defined test wavelengths and validated assays to deliver accurate measurements. Users should run routine quality control materials, follow calibration procedures, and adhere to the laboratory’s quality management policies to maintain result reliability.

As a Class II clinical instrument, the H-100 should be operated by trained personnel. Follow biosafety procedures for handling urine samples, use appropriate personal protective equipment, and adhere to the safety instructions in the device manual.

The H-100 provides quantitative spectrophotometric measurements for its specified analytes. For detailed performance characteristics (limits of detection, linear ranges and reference intervals), consult the product specifications and validation documents.

The H-100 is manufactured in Jiangsu, China. For sales, service, parts and technical support, contact Dirui or an authorized distributor in your country. Your supplier can provide pricing, delivery, installation and service contract information.