What is the maximum operating time?

The time range is adjustable up to 9999 minutes.

What is the electrical requirement?

The electrical requirement is 220V 50Hz.

Chinese Cost-Effective Forced Air Drying Oven with CE Certificate

Name: Chinese Cost-Effective Forced Air Drying Oven with CE Certificate
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 706984142

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

Negotiable

1 Piece

Product profile

Customization

Available

Heating Mode

Convective

Drying Medium

Air

Model NO.

HP-9070I

Operation Pressure

Atmospheric Dryer

Operational Method

Continuous

Model

HP-9070I

Interior Dimension(Wxdxh,mm)

450X400X450

Exterior Dimension(Wxdxh,mm)

740X618X630

Shleves(Optionable)

Electrical Requirements

220V 50Hz

Structure

Air Flow Drier

Transport Package

Neutral Exporting Package

Specification

CE/SGS/GMP/ISO

Trademark

HEPOBIO

Origin

China

Production Capacity

1200units/Month

Key features

Dual Display Feature: Double color display shows set and real-time chamber temperature.

CE Certified Safety: Series holds CE certificate for compliance and safety standards.

Automatic Over-Temp Protection: Automatically stops operation if temperature exceeds limits.

Fahrenheit Option: Controller can be changed to Fahrenheit for display and control.

Programmable Timer: Time range adjustable from 1 to 9999 minutes.

Customizable Shelves: Includes 2 optional shelves for flexible interior arrangement.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.80h

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.