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China Manufacturing Laboratory Semi-Auto Chemistry Analyzer
US$500.00-1,100.00
1 Piece

Product profile

Customization

Available

Classification

Biochemical Apparatus

Type

Biochemistry Analyzer

Model NO.

HP-SCHEM300

Certification

CE, FDA, MSDS, ISO13485

Group

Middle-aged and Old

Light Source

6V/10W Tungsten Halogen Lamp

Standard Wavelength

340,405,510,578,630,690nm

Flow Cell

32UL Quartz Flow Cell

Dimensions

430(L)*330(W)*140(H)mm

Net Weight

7.0kg

Analysis Means

End-Point, Kinetic, Fixed-Time, Nonlinear

Minimun Volume

200ml~3000ml

Storage

200 Test Parameters and up to 20000 Sample Results

Interface Connections

PS/2, USB, RS-232, Parallel Rort

Read-Range

0.000~3.000ABS

Transport Package

Exporting Wooden Package

Specification

CE SGS ISO9001 ISO13485 FDA

Trademark

HEPOBIO

Origin

China

HS Code

9027809900

Production Capacity

1000 Sets Per Month

Key features

High-Resolution Touch Screen: Features a 5.7-inch high-resolution LCD display with optional external mouse and keyboard support.
Precise Temperature Control: Micro dimension flow cell ensures precise temperature control at 25, 30, and 37 degrees Celsius.
Large Data Storage Capacity: Stores up to 200 test parameters and 20,000 sample results with result correction capabilities.
High Reproducibility: Ensures high reproducibility with a deviation of less than 1.0% for accurate test results.
Multiple Analysis Modes: Supports End-Point, Kinetic, Fixed-Time, and Nonlinear analysis methods for versatile testing.
Comprehensive Certifications: Certified with CE, FDA, MSDS, and ISO13485 standards for global market compliance.
Real-Time Monitoring: Displays real-time reaction curves during tests for timely detection of abnormal conditions.
Compact and Lightweight: Compact dimensions of 430x330x140mm and a net weight of only 7.0kg for easy placement.

Company profile

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.

Product Q&A

Q:What are the standard wavelengths available?
A:
The standard wavelengths are 340, 405, 510, 578, 630, and 690 nm.
Q:What is the minimum sample volume required?
A:
The minimum volume ranges from 200ml to 3000ml depending on the specific test requirements.
Q:Does the analyzer support external software integration?
A:
Yes, it supports intercommunication via RS-232 and optional Lead-Workstation biochemistry analyzing software.
Q:What certifications does the HP-SCHEM300 have?
A:
The device is certified with CE, FDA, MSDS, and ISO13485 standards.
Q:What is the stability of the analyzer?
A:
The stability is within 0.01A, ensuring consistent performance over time.

Send Inquiry

*To:Zhengzhou Hepo International Trading Co., Ltd.Zhengzhou Hepo International Trading Co., Ltd.
*Content:
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