Latest Factory Price Pharmaceutical Stability Testing Chamber with UV Sterilization

Name: Latest Factory Price Pharmaceutical Stability Testing Chamber with UV Sterilization
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 765964495

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

Negotiable

1 Piece

Product profile

Customization

Available

Customized

Structure

Desktop

Model NO.

HP-PST160

Material

Stainless Steel

Certification

CE, ISO

Application

School, Hospital, Lab

Type

Incubator

Capacity

160L

Temperature Range

0~65℃

Temperature Balanced

±0.5℃

Inner Chamber Size

560*410*670

Power

2200W

Display

Programmable LED Display & LCD Touch Screen(Option

Transport Package

Standard Export Packing

Specification

CE/SGS/GMP/ISO

Trademark

HEPOBIO

Origin

China

Production Capacity

10000sets/Year

Key features

Dual Compressor System: Two imported compressors switch automatically to ensure continuous, long-term operation without failure.

UV Sterilization Option: Optional UV lamp kills floating bacteria and prevents pollution during drug stability tests.

Multi-Scenario Application: Suitable for pharmaceutical stability, food quality, environmental testing, and microbial culture.

Advanced Touch Control: Optional LCD touch screen with 100 groups, 1000 segments, and 999 cycles for easy programming.

Data Recording & Alarm: Built-in printer, RS-485 interface, and independent temperature/humidity limit alarm system.

Easy to Clean Design: 304 stainless steel liner with semi-circular arc corners ensures hygiene and ease of maintenance.

CE & ISO Certified: Meets international safety and quality standards with CE and ISO certifications.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.59h

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.