Is LIS integration available?

Yes, it is available for LIS via RS232, PS/2, and USB outputs.

What languages does the system support?

It comes with English and Spanish, with other languages available on request.

What is the lead time for orders?

Peak season lead time is 6-12 months, while off-season is within 15 workdays.

China Auto Parts Three Part Diff 22 Parameters Hematology Analyzer

Name: China Auto Parts Three Part Diff 22 Parameters Hematology Analyzer
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 770519995

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$1,000.00-3,170.00

1 Piece

Product profile

Customization

Available

Classification

Imaging Diagnostic Equipment

Type

Biochemistry Analyzer

Model NO.

HP-HEMA6500B

Certification

CE, ISO13485

Group

Middle-aged and Old

Aautomatic

Full Automatic

Throughput

60test/H

Assay Items

22 Parameters, 3 Parts Different of Wbc

Sample Volume

13UL (Whole Blood ), 20UL(Prediluted Blood)

Mearsuring Principle

Electro-Imprdance, Photometric Analysis

Display

10' LCD

External Dimension

43cm*32cm*50.5cm

Net Weight

20.00kg

Storage

200,000 Results Including Histograms

Output

One RS232, One PS/2 and Two USB. Avaliable for Lis

Transport Package

Standard Packing

Specification

CE ISO

Trademark

HEPOBIO

Origin

China

HS Code

9027809900

Production Capacity

4500 Sets/Month

Key features

22 Parameters Analysis: Comprehensive 3-part differential WBC analysis with 22 specific parameters.

High Throughput Speed: Processes up to 60 tests per hour for efficient laboratory workflow.

Dual Sample Mode: Supports both whole blood (13uL) and prediluted blood (20uL) testing.

Advanced Washing System: Automatic probe interior and exterior washing prevents carry-over contamination.

Large Data Storage: Stores 200,000 results including histograms for extensive record keeping.

Comprehensive Connectivity: Equipped with RS232, PS/2, and USB ports for LIS integration.

Built-in Thermal Printer: Includes internal printer with option for external USB connection.

Multi-language Support: Standard English and Spanish with additional languages available on request.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.54h

AI-Powered supplier vetting

SummaryThe supplier presents established manufacturing and quality-system credentials, with eight production lines, stated output across five medical-equipment categories, broad export coverage, and ISO 13485, ISO 9001, ISO 14001, and GMP certifications. It offers extensive product customization and maintains inventory capability, with stated lead times within 15 working days in both peak and off-season periods. However, evidence also shows material gaps: no written corrective-action or complaint-handling procedures, no documented service-assessment procedure, no environmental impact assessment report, no overseas warehouse or showroom, no recent new-product activity, no ODM or major-brand OEM service, no SDK, zero stated R&D patents, and no available R&D design-control documentation. Financial records are indicated for multiple years, but the slices do not provide sufficient non-financial evidence to assess financial credibility.

Supplier typeThe supplier manufactures medical and biosafety-related equipment, including cold-chain, clinical, first-aid, and laboratory products. It operates eight production lines, describes imported production equipment, and exports to multiple global regions, indicating a manufacturer with broad product and market coverage.

CertificationsThe supplier states that its factories adopted ISO 9001:2008 and ISO 13485 systems, while its supplier-management certifications include ISO 13485, ISO 9001, ISO 14001, and GMP. These explicitly stated certifications support a positive assessment of formal quality and management-system coverage.

R&D capabilityThe supplier has 11–20 years of total R&D-engineer experience and can customize products, but reports no new products during the past year, no SDK, no software-instrument R&D, zero R&D patents, and no available design-input, output, review, verification, or validation documentation. The explicit evidence indicates limited demonstrated innovation infrastructure.

Production capacityThe supplier operates eight production lines and reports production quantities for deep freezers, analyzers, and incubators, alongside inventory capability and broad export markets. Its company description also cites dedicated product solutions and imported production equipment, providing explicit evidence of substantial manufacturing capability.

Customization capabilityThe supplier explicitly offers customization from samples and designs, full, minor, and flexible customization, and assigns R&D engineers to customize products according to customer needs. However, the absence of documented R&D design-control records means process formalization is not demonstrated, while the customization offering itself is clearly supported.