Russian Software Hospital Semi Automatically Biochemistry Analyzer

Name: Russian Software Hospital Semi Automatically Biochemistry Analyzer
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 701542532

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

US$950.00-1,150.00

1 Piece

Sample price:US$1150.00/piece.Request sample

Product profile

Customization

Available

Classification

Biochemical Apparatus

Type

Biochemistry Analyzer

Model NO.

HP-CHEM3200S

Certification

CE, ISO13485

Group

Middle-aged and Old

Reading Cuvette

Both Flow Through Cell and Direct Reading Cuvette

Measuring Volume

200UL-800UL

Pre-Incubator

20incubating Positions

Photometric System

6V/100W Halogen Lam

Wavelength Filter

340/405/492/510/546/578/620nm,9 Filters Can Be Ok

Interface

RS-232 Serial Port, USB Port

Thermostatic Control

25c,30c,37c

Thermostatic Precision

0.1c

Measuring Principle

End Point, Fixed Time,Multistandsrd, Bichromic and

Photometric Linearity

2%,0 to 3.000 O.D

Test Menu

T.Bili,Tp,Alp,Ast/Got,Glu,Alt/Gtp,etc

Quality Control

Q.C. Chart May Be Displayed and Printed

Display Screen

5inch Back-Illuminated LCD

Patient Storage

Over 200 Programs, 1000 Teat Results

Printer

Built-in Thermal Printer

Transport Package

Carton or Wood Package

Specification

Color Touch Screen

Trademark

HEPOBIO

Origin

China Henan

HS Code

9027809900

Production Capacity

2300sets/Month

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤1.80h

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.