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Full Automatic 8 or 12 Channel Modes Microplate Washer

Name: Full Automatic 8 or 12 Channel Modes Microplate Washer
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 717220042

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$1,410.00

1 Piece

Product profile

Customization

Available

Classification

Biological Diagnostics

Type

Biochemistry Analyzer

Model NO.

HP-MW5000

Certification

CE, ISO13485

Group

Middle-aged and Old

Dimensions

48*40*27cm

Weight

6.0kg

Power Supply

AC 110V/60Hz or 220V/50Hz

Display

Back-Illuminant LCD

Storage

50 Programs

Self-Test Function

Automatic Location Check

Alarming

Automatic Alarm After Washing

Wash Cycles

0-99

Transport Package

Stardard Exporter Package

Specification

48*40*27cm

Trademark

HEPOBIO

Origin

China

HS Code

9027899090

Production Capacity

2000 Sets Per Month

Key features

Dual Channel Modes: Available in 8 or 12 channel modes for flexible microplate washing.

High Precision Dispensing: Dispensing precision under 2%CV at 300ul across the plate.

Low Residual Volume: Achieves residual volume of less than 2ul per well.

Automatic Self-Test: Features automatic location check for reliable operation.

Large Program Storage: Capable of storing up to 50 different washing programs.

Multi-Interface Support: Equipped with RS232 and USB ports for data connectivity.

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

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.52h

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.