Can the device record test data?

Yes, it can connect to a printer or use RS-485/232 interfaces to record temperature and time curves for data storage.

What materials are used for the interior?

The interior liner is made of 304 stainless steel with semi-circular arc corners for easy cleaning.

GMP Certification Pharmaceutical Stability Testing Incubator with Factory Price

Name: GMP Certification Pharmaceutical Stability Testing Incubator with Factory Price
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 742645335

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

Negotiable

1 Piece

Product profile

Customization

Available

Application

Industry, School, Hospital, Lab

Customized

Model NO.

HP-PST270

Certification

CE, GMP

Structure

Desktop

Material

Stainless Steel

Type

Incubator

Net Capacity

270L

Temperature Range

0 ~ 65℃

Humidity Control

40~95%Rh,±3%Rh

Illumination

0 ~ 6000lux

Inner Size(WDH)

605*503*850

External Size(WDH)

745*900*1700

Transport Package

Standard Export Package

Specification

CE/SGS/GMP/ISO

Trademark

HEPOBIO

Origin

China

Production Capacity

1000-2000units

Key features

GMP & CE Certified: Meets strict GMP and CE certification standards for pharmaceutical stability testing.

Continuous Operation: Dual imported compressors switch automatically to ensure uninterrupted long-term testing.

Stainless Steel Build: Constructed with 304 stainless steel liner and semi-circular arc corners for easy cleaning.

Smart Data Recording: Supports printer and RS-485/232 interfaces for data storage, playback, and fault diagnosis.

Safety Alarms: Features independent temperature/humidity limit alarms and sound/light alerts for safety.

UV Sterilization: Optional UV system effectively kills floating bacteria and prevents pollution during tests.

Customizable Options: Offers customizable net capacity, temperature range, humidity control, and illumination levels.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤2.54h

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.