Is the device easy to operate?

Yes, it features automatic self-checking, warming, and standby functions for ease of use.

What certifications does the product have?

It is certified with CE, FDA, and ISO13485.

What languages are supported?

English and Spanish are standard, with other languages available on request.

3 Diff 22 Parameters Color Touch Screen Auto Hematology Analyzer

Name: 3 Diff 22 Parameters Color Touch Screen Auto Hematology Analyzer
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 708334982

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$2,000.00-4,000.00

1 Piece

Product profile

Customization

Available

Classification

Physiological Functions of Diagnosis and Monitoring Equipment

Type

Urine Analyzer

Model NO.

HP-HEMA6500B

Certification

CE, FDA, ISO13485

Group

Middle-aged and Old

Test Parameters

3-Part Diff, 22 Parameter

Screen Size

10.4 Inch

Storage

20k

Power

50Hz&Plusmn3Hz

Analyzer Packing Dimension(mm)

530*466*595

Weight

Nw:20kg, Gw: 24kg

Free Reagents Packing

360*300*280mm

Test Item

Wbc,Rbc,Hgb,Plt,Mcv

Sample Volume

Twig Blood: 20UL

Test Speed

60 Samples/Hours

Transport Package

Standard Packaging

Specification

ISO9001: 2008 ISO13485 CE SGS

Trademark

hepomed

Origin

China

HS Code

9027809900

Production Capacity

350 PCS/Month

Key features

22-Parameter Analysis: Detects 3-part diff WBC, RBC, HGB, PLT, and 18 other parameters with high accuracy.

High Throughput Speed: Processes up to 60 samples per hour for efficient clinical laboratory workflows.

Dual Test Mode Support: Supports both whole blood and prediluted blood testing modes for flexibility.

Advanced Carry-Over Protection: Features automatic probe interior and exterior washing to prevent sample contamination.

Large Data Storage: Stores up to 200,000 results including histograms for comprehensive record keeping.

Multiple Connectivity Options: Equipped with RS232, PS/2, and two USB ports for LIS integration and data output.

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

CE, FDA, ISO13485 Certified: Meets international safety and quality standards for medical diagnostic equipment.

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.