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Nanjing Laola Electronic Co., Ltd. markets the Faith-1020 biochemical analyzer, an automatic random access system designed for clinical and research laboratory environments. The instrument processes multiple samples simultaneously with throughput capacity for high-volume workflows, integrating with laboratory information management systems (LIMS) for data handling. The supplier emphasises calibration and diagnostic features intended to maintain consistent analytical performance across assay runs.
Random access architecture allows the Faith-1020 to prioritise urgent samples without disrupting scheduled test sequences, a critical capability for emergency laboratory medicine. The system likely employs photometric measurement methods, standard for clinical chemistry analyzers in this class, though the exact wavelength range and optical path length are not detailed in the source. Typical biochemistry analyzers at this throughput level operate with reaction volumes of 150-350 microlitres, with temperature-controlled cuvette blocks maintained at 37 degrees Celsius plus or minus 0.1 degrees for enzyme-based assays. Reagent refrigeration and on-board stability specifications would be essential verification points for prospective buyers.
Target buyers include hospital clinical laboratories, independent diagnostic centres, and research institutions requiring quantitative analysis of blood, serum, plasma, or urine analytes. The Nanjing location places the supplier within the Yangtze River Delta manufacturing corridor, with access to Shanghai Pudong International Airport and Shanghai Port for international shipment. The listing mentions flexible minimum order quantities and FOB or CIF shipping terms, though exact figures require direct confirmation. ISO certification references appear in the source description, but specific certificate numbers and scopes need validation before purchase commitment.
| Product Model | Faith-1020 |
| System Type | Automatic random access biochemical analyzer |
| Throughput | Multiple samples simultaneously (exact tests/hour not specified) |
| Software Interface | User-friendly interface (supplier description) |
| LIMS Integration | Compatible with various laboratory information management systems |
| Calibration Features | Advanced calibration and diagnostic features (supplier description) |
| Typical Reaction Volume | 150-350 µL (standard for this analyzer class) |
| Typical Reaction Temperature | 37 ± 0.1 °C (standard for enzyme-based clinical chemistry) |
| Typical Wavelength Range | 340-800 nm (standard photometric range for clinical analyzers) |
| Typical Sample Rack Capacity | 60-100 positions (standard for compact-to-mid throughput systems) |
Nanjing Laola Electronic Co., Ltd. operates from High Technology Park #1 Guanghua Road, Baixia District, Nanjing 210014, Jiangsu Province, China. The supplier holds an imported tier designation alongside harbor trust tier, suggesting the product may originate from a different manufacturer or the company imports components for assembly. The response rate is recorded at 0.00% with zero average response hours, indicating no platform-mediated communication history. Buyers should not interpret this as negative verification but should prepare for potentially slow initial responses and consider direct contact methods.
The company profile does not disclose establishment year, registered capital, employee count, annual revenue, R&D expenditure, or specific factory floor space. No information details previous export markets, installed base size, or customer references. The source description attributes several capabilities to the product, but buyers must independently verify ISO certification scope (ISO 13485 for medical devices is particularly relevant), whether any FDA registration exists and its 510(k) status if applicable, and the actual manufacturing location of the Faith-1020. Request a copy of the quality management system certificate, business licence, and any medical device registration certificates held in China (NMPA registration) or target export markets.
| Business Type | Supplier |
| Year Established | Recently Joined |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| Response Time | Contact Supplier |
| Response Rate | New Supplier |
Before committing to purchase, verify Nanjing Laola Electronic Co., Ltd.'s business registration with the Jiangsu Administration for Market Regulation and confirm the company's manufacturing or trading status. For medical device procurement, request the National Medical Products Administration (NMPA) registration certificate for the Faith-1020, as export of unregistered medical devices from China carries compliance risks. Validate any claimed ISO 13485 certificate directly with the certification body using the certificate number. Inspect the manufacturing facility or engage a third-party auditor to assess production capabilities, quality control processes, and whether the company manufactures the analyzer or trades under another manufacturer's OEM arrangement.
Logistics planning requires clarification of whether shipment is from Nanjing Lukou International Airport air freight, Shanghai Port sea freight, or another export gateway. For a precision instrument like a biochemical analyzer, air freight is strongly preferred despite higher cost, as sea freight vibration and humidity exposure risk optical and electronic component damage. Negotiate Incoterms with this in mind: DAP (Delivered at Place) to your facility places transport risk on the seller, while EXW (Ex Works) from Nanjing requires you to arrange all export logistics. For payment, letters of credit provide security for both parties on first transactions, though Chinese suppliers often prefer T/T advance. Lead time, production scheduling, and whether the Faith-1020 is stocked or built-to-order must be confirmed directly with the supplier.
Quality assurance on receipt involves unpacking inspection for shipping damage, verification of voltage and frequency compatibility, and commissioning with calibration verification materials. Request factory acceptance test (FAT) documentation and plan for site acceptance testing (SAT) with your laboratory's assay panel. Verify that reagent formulations and control materials for your intended test menu are available in your country, as reagent supply continuity determines long-term instrument utility. Establish a preventive maintenance contract or identify qualified local biomedical engineering support, as analyzer downtime directly affects laboratory throughput. For regulatory compliance in your jurisdiction, confirm that the Faith-1020 meets electrical safety (IEC 61010-1), electromagnetic compatibility (IEC 61326), and in vitro diagnostic directive requirements applicable to your import country.
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