20L Handable Ice Lined Cooling Storage Transport Box

Name: 20L Handable Ice Lined Cooling Storage Transport Box
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 805944285

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$120.00-490.00

1 Piece

Sample price:US$390.00/piece.Request sample

Product profile

Customization

Available

Customized

Certification

CE, FDA, EEC, ISO13485

Model NO.

HP-CL20E

Scale

Small

Over-Temperature Alarm

with Alarm Function

Type

Medical Cryostat

Cooling Temperature

2 to 8 Centigrade

Cooling Time

24hours to 72hours Accordingly

Cooling Source

Ice Bricks or Bags

Thick Insulation

PU Foaming

Thermal Display

Temperature Digital Display

Innser Size

375*215*250

External Size

425*265*305

Net Weight

3kgs

Shelve

One

Shoulder Belt

One

Transport Package

Carton Standard Package

Specification

20Liters, 18Liters

Trademark

HEPOBIO

Origin

China

HS Code

3923100090

Production Capacity

5000units/Month

Key features

Durable Construction: High impact seamless double walled design with stainless steel latches.

Eco-Friendly Materials: Made of non-toxic, UV resistant, and corrosion-resistant PU foaming.

Multiple Certifications: Certified by CE, FDA, EEC, and ISO13485 for medical use.

Convenient Drainage: Features a recessed drain plug system for easy melted ice removal.

Secure Transport: Includes padlock holes and non-slip design for stability.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.52h

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.