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Intelligent Control Constant Temperature and Humidity Incubator
US$1,020.00-1,288.00
1 Piece

Product profile

Customization

Available

Application

Industry, School, Hospital, Lab

Customized

Customized

Model NO.

HP-CTHI380

Certification

CE, ISO, SGS

Structure

Desktop

Material

Stainless Steel

Type

Incubator

Capacity

380L

Temperature (℃)

0-60

Humidity (%Rh)

50-95

Chamber Size(mm)

505*505*1380

External Size(mm)

605*605*1950

Alarm

High and Low Temperature Humidity

Printer

Build in Thermal Printer

Computer Port

RS485 or RS232 Port with Software

Control System

LCD Computer Micro Countrol

Transport Package

Standard Package

Specification

CE, SGS

Trademark

HEPOBIO

Origin

China

HS Code

8514109000

Production Capacity

10000~20000/Year

Key features

Versatile Applications: Suitable for plant germination, microbial culture, insect breeding, and research.
Advanced Safety Features: Includes alarms for temp/sensor failure, power-off memory, and independent limit alarms.
Smart Control System: LCD touch control, 30 programmable segments, RS485/RS232 port with software.
Quality Components: Uses original SECOP compressors, hollow reflective tempered glass, and built-in printer.
Customizable Options: Offers customized capacity, door types (glass/metal), and optional accessories.
Professional Support: International sales and aftersales team providing training and technical solutions.
Certified Quality: Products certified with CE, ISO, and SGS standards for global compliance.

Company profile

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.

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