Stock Supply China 4liters Vaccine Transfer PU Insulation Passive Cold Cool Boxes

Name: Stock Supply China 4liters Vaccine Transfer PU Insulation Passive Cold Cool Boxes
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 811351785

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$49.00-93.00

10 Pieces

Sample price:US$90.00/piece.Request sample

Product profile

Customization

Available

Capacity

3L to 1000liters

Color

Black, Blue, Gray, Green, Orange, Pink, Purple, Red

Model NO.

HP-CPL5

Material

Polyethylene

Soaking Time

>6H

Temperature Range

2℃ to 8℃

Usage Scenarios

Food Delivery, Frozen Food Transport, Medical Supplies Transport, Pharmaceutical Transport

Cooling Source

Ice Bricks or Ice Bags

Outside Raw Materals

Polyethylene(HDPE)

Inner Lining Raw Materials

Polystyrol(PS)

Thmeral Display

Temperature Digital Display Screen

Lid

Self-Lock Style

Transport Package

Strength Carton Package

Specification

280*220*190mm

Trademark

HEPOBIO

Origin

China

HS Code

39269010

Production Capacity

100000 Pieces Per Month

Key features

HEPO portable cool box is designed for supplying 8hours to 48hours long time cooling and freezing usage.

Cooling Temperature range can be 0 to 10degree,-15degree,-20degree or wider.

Convenient handles and shoulder belt designing for easy to carry and handle.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤3.34h

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.