2-8degree Mini Medical Refrigerator with Good Quality (48L)

Name: 2-8degree Mini Medical Refrigerator with Good Quality (48L)
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 694444072

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$395.00-425.00

5 Pieces

Product profile

Customization

Available

After-sales Service

Online Video or Phone

Warranty

One Year

Model NO.

HP-5V48

Capacity

50L

Door Number

Single Door

Type

Upright Freezer

Door Type

Sliding Door

Power Source

Electricity

Temperature Control

Computer Thermostat

Defrost Type

Auto Defrost

Function

Cold Storage

Certification

CE, ISO

Model

HP-5V48

Voltage (V/Hz)

220/50

Power(W)

Temp

2~-8(Oc)

N.W.

4.5kgs

Transport Package

Standard Packing

Specification

450*450*575mm

Trademark

hepomed

Origin

Zhengzhou of Henan

HS Code

84185000

Production Capacity

1000units

Key features

Comprehensive Safety: Features buzzer, flashing light, remote warning, and password lockout.

Energy Efficient Cooling: Uses famous branded compressor and non-CFC high-efficiency refrigerant.

Versatile Application: Ideal for storing vaccines, blood, and biological products in labs or hospitals.

Compact Design: Lightweight and small volume, suitable for tabletop or under-counter placement.

Wide Voltage Range: Operates stably within 198-242V to adapt to different power environments.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤2.89h

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.