自动分析仪

Automated Analyzers

Photo for reference; configuration may vary by order.

Model No. AUA-0004 · Laboratory Automation

Batch Automated Analyzer

批量自动分析仪

Where samples arrive in groups, such as food plants or industrial QC labs, batch analysis keeps calibration simple. This analyzer processes 20–200 samples per batch at 100–600 tests/h, using 5–500 µL per test. Calibration can run per batch or on schedule, QC positions are user defined, and photometric reads follow a fixed 37 °C incubation.

Type: Batch automated analyzer
Throughput: 100–600 tests/h
Batch size: 20–200 samples
Sample volume: 5–500 µL per test
Calibration: Per batch or schedule

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Packing & Shipping

Place of origin	China (dispatched from Shanghai)
Brand	Liquid International / OEM on request
Export packing	Fumigation-free plywood case or reinforced carton
Loading port	Shanghai / Ningbo (others on request)
Payment terms	T/T, L/C at sight (confirmed on quotation)
Trade terms	EXW, FOB, CFR, CIF, DAP

Typical export terms — final terms are confirmed on the proforma invoice.

Product Description 产品描述

Highlights

Batches of 20–200 samples at 100–600 tests/h
Sample volume 5–500 µL per test
Calibration per batch or on a set schedule
User-defined QC positions and fixed 37 °C incubation

Applications

Food and beverage testing
Environmental batch analysis
Industrial QC
Dedicated routine assays

Specifications 技术参数

Parameter	Value
Type 类型	Batch automated analyzer
Throughput 通量	100–600 tests/h
Batch size 批量	20–200 samples
Sample volume 样品体积	5–500 µL per test
Calibration 校准	Per batch or schedule
QC positions 质控位	User defined
Incubation 孵育	Fixed cycle, 37 °C
Detection 检测	Photometric
Flexibility 灵活性	Low per-sample variation
Data export 数据导出	LIS or file export
Model No.	AUA-0004
Place of origin	China (dispatched from Shanghai)

Applicable standards 适用标准

IEC 61010-1 (safety requirements for electrical equipment) ISO 15189 (medical laboratories, quality and competence) ISO 17511 (traceability of calibrators and control materials) EU IVDR (in vitro diagnostic medical devices) 21 CFR Part 11 (electronic records and signatures) CLIA (clinical laboratory improvement requirements)

Chinese national standards (GB/T, JJG) and international standards referenced for this product type. Test reports and certificates are supplied with the quotation on request.