Medical Portable 2D/3D Digital Color Doppler Machine (HP-UC610PLUS)

Name: Medical Portable 2D/3D Digital Color Doppler Machine (HP-UC610PLUS)
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 716612192

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$5,260.00-8,350.00

1 Piece

Sample price:US$5470.00/piece.Request sample

Product profile

Customization

Available

Classification

Imaging Diagnostic Equipment

Type

Ultrasound Scanner

Model NO.

HP-UC610PLUS

Certification

CE, MSDS, ISO13485

Group

Middle-aged and Old

Software

Windows 7 Embedded Operating Platform

Build-in Back up Battery

More Than 3 Hours Lithium Battery

Imaging Element

128 Array Element System and Probe

Warranty

24 Month

Probe Element

128

Probe

1 Probe Socket,

Operation Interface

Win 7

System Language

English and Other 11 Kinds for Select

Display Mode

B,B+B,4b,B+M,M,C,Pw,Cw,B/C,B/C/Pw

Focus

More Than 57

Image Processing

up/Down, Left/Right, Angular Variation, Reverse

Measurement

Distance, Circumference, Area, Volume, Heart Rate

Application

Abdomen,Cardiac,Skeletal Muscle, Early Obstetrics,

Cine Loop

More Than 1200 Frames

Puncture Guide

Available to Set Accordingly

Transport Package

Exporting Carton Package

Specification

15 inch LED medical display monitor

Trademark

HEPOBIO

Origin

China

HS Code

9018121000

Production Capacity

2000 Sets Per Month

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.62h

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.