What is the response time for after-sales service?

A positive response is provided within 24 hours via phone, email, or other means.

What are the power supply requirements?

The device supports AC 110V 60HZ or 220V 50HZ power supply.

What is the lead time for delivery?

Off-season lead time is within 15 workdays, while peak season lead time is 6-12 months.

Peru Popular Lab 3 Part Difference Hematology Analyzer

Name: Peru Popular Lab 3 Part Difference Hematology Analyzer
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 703794172

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$1,000.00-3,000.00

1 Piece

Product profile

Customization

Available

Classification

Imaging Diagnostic Equipment

Type

Urine Analyzer

Model NO.

HP-HEMA6500A

Certification

CE, ISO13485

Group

Middle-aged and Old

Aautomatic

Full Automatic

Assay Items

3 Diff, 22 Parameters

Throughput

60test/H

Sample Volume

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

Mearsuring Principle

Electro-Imprdance, Photometric Analysis

Data Input

Keypad

External Dimension

43cm*32cm*50.5cm

Net Weight

20.00kg

Display

7 Inch; LCD

Storage

200, 000 Results Including Histograms

Transport Package

Standard Exporting Carton Package

Specification

CE, ISO, SGS

Trademark

HEPOBIO

Origin

China

Production Capacity

5000pieces Per Month

Key features

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

Versatile Sample Modes: Supports both whole blood and prediluted blood testing modes.

Large Data Storage: Stores up to 200,000 results including histograms for easy retrieval.

Comprehensive Parameter Analysis: Measures 22 parameters including 3-part WBC differential.

Advanced Safety Features: Features carry-over protection via automatic probe washing.

Lifetime Technical Support: Provides lifetime paid maintenance and technical support post-warranty.

CE and ISO13485 Certified: Meets international standards for medical device quality and safety.

Built-in Thermal Printer: Includes a built-in thermal printer for immediate result printing.

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.