Lab Constant Temperature Biological Cell Growth Incubator (HP-CTB180)

Name: Lab Constant Temperature Biological Cell Growth Incubator (HP-CTB180)
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 740381925

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$1,010.00-1,160.00

1 Piece

Sample price:US$1100.00/piece.Request sample

Product profile

Customization

Available

Application

Industry, School, Hospital, Lab

Customized

Model NO.

HP-CTB180

Certification

CE, ISO

Structure

Desktop

Material

Stainless Steel

Type

Incubator

Capacity

180liters

Temerature Accurency

1centigrade

Temperature Control

Microcomputer

Programmable

30 Multi-Paragraph Control Mode Is Optional

Displaying

Digital LED Display or LCD,Double Displaying

Timer

0-9h or Continuous

Alarm

Sound and Light Alarm

Compressor

Sealed Secop

Cooling Agent

R12 (Normal) R134A(Environment Protection Type)

Door

Painted Steel with Window or Full Glass Door

Protect Function

Temeprature,Start Delay Function,Pressure

Inner

304 Stainless Steel Inner

Illumination

Yes

Shevles

304 Stainless Steel

Remote Alarm

Available

Transport Package

Export Plywood Case

Specification

0C to 50C or 60Centigrade

Trademark

HEPOBIO

Origin

Henan of China

HS Code

8419899090

Production Capacity

2000/Month

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.84h

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.