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New 4D Color Doppler Ultrasound System (HP-UC800)

Name: New 4D Color Doppler Ultrasound System (HP-UC800)
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 712319632

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$2,000.00-5,000.00

1 Piece

Product profile

Customization

Available

Customized

Non-Customized

Certification

CE, ISO13485

Model NO.

HP-UC800

Scale

Medium

Probe Element

Monitor

15 Inch LED Monitor

Probe Socks

Equipment Weight

45kg

Sostware

3D Workstation

Warranty

24 Month

Transport Package

Standard Export Package

Specification

CE ISO13485 FDA

Trademark

HEPOBIO

Origin

China

HS Code

9018121000

Production Capacity

100 Sets Per Month

Key features

Comprehensive Software Packages: Includes OB, GYN, Small parts, Urology, Anthology, Cardiac, and Vessel analysis software.

Advanced Imaging Processing: Features Tissue Harmonic, Speckle reduction, and Multi beam parallel processing technologies.

15-Inch LED Monitor: Standard 15-inch high resolution LED monitor with PC LED backlit silicon gel keyboard.

Multiple Operating Modes: Supports B, 2B, 4B, B/M, M, B/C, B/C/D, B/D, PW, velocity, and power histogram modes.

CE and ISO13485 Certified: Meets international safety and quality standards with CE and ISO13485 certifications.

24-Month Warranty: Comes with a 24-month warranty coverage for peace of mind and reliability.

Compact and Portable Design: Equipment size 880x580x1400mm, weight 45kg, designed for easy mobility in clinics.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.59h

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.