China Quality -86centigrade Chest Ultra-Low Temperature Sharp Freezer

Name: China Quality -86centigrade Chest Ultra-Low Temperature Sharp Freezer
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 704856512

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$2,000.00-2,650.00

1 Piece

Sample price:US$2250.00/piece.Request sample

Product profile

Customization

Available

After-sales Service

Online/Video/Phone

Warranty

One Year

Model NO.

HP-86C210E

Capacity

201-250L

Door Number

Single Door

Type

Chest/Deep Freezer

Door Type

Swing Door

Power Source

Electricity

Temperature Control

Smart Thermostat

Temperature Type

Single-temperature

Defrost Type

Frost-Free

Function

Cold Storage & Freezing, Freezing, Cold Storage

Certification

CE, RoHS, ISO, CCC, CB, SASO, EMC, GS, ETL

Temperature Control Range

-40degree to -86centigrade

Inside Liner

Stainless Steel

Lock & Key

Yes

Rated Input Power

550W

Refrigerant

CFC Free

Compressor

Secop or Same Grade Brand

Temperature Display

Digital Display

Heated Frame Door

Avoid Door Seal Iced

Inner Size(WDH)

849*468*640mm

External Dimension

1100*680*800mm

Transport Package

Strength Exporting Package

Specification

120Liters

Trademark

HEPOBIO

Origin

China

HS Code

84183010

Production Capacity

1200units Per Month

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.92h

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.