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Human Immunodeficiency Virus Type 1 Nucleic Acid Detection Kit (Fluorescence PCR Method)
US$9.20-10.00
1 Piece

Product profile

Customization

Available

Type

IVD Reagent

Wide linear range

30~1.0×10^8 IU/mL

Model NO.

P867H/P868H

Spec

P867H/P868H

Shelf Life

12 Months

Specimen

Human serum/plasma

Analysis Method

Quantitative Analysis (Internal Standard Method)

LoD

12.5 IU/mL

LoQ

30 IU/mL

Transport Package

Paper Carton

Specification

57*42*32 cm

Trademark

Tianlong

Origin

Xi'an Shaanxi

Production Capacity

5000000 Test/Year

Key features

High Sensitivity Detection: Limit of Detection (LoD) as low as 12.5 IU/mL for accurate viral load assessment.
Broad Genotype Coverage: Detects all major Hepatitis C Virus genotypes 1 through 6.
Accurate Quantification: Uses internal standard method to minimize inter-tube variation and ensure reliability.
Anti-Contamination Design: Incorporates UNG-dUTP technology to reduce contamination risks.
High Clinical Accuracy: Achieved 100% positive and 99.43% overall coincidence rates in clinical trials.
Flexible Customization: Offers full, minor, and flexible customization options from samples or designs.
Integrated Solution: Provides comprehensive solutions including extraction, setup, and detection options.

Company profile

Xi'an Tianlong Science and Technology Co., Ltd.
Importers and ExportersHigh Repeat Buyers ChoiceExhibition ExperienceYears of Export Experience
Business Type: Manufacturer/Factory CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 20 years CertifiedNearest Port: Shenzhen Port, Shanghai PortAverage Response Time: ≤2.00h

AI-Powered supplier vetting

SummaryTianlong demonstrates established quality and management credentials, including ISO 13485, ISO 9001, ISO 14001, and ISO 45001:2018-related certifications. Its documented supplier-service procedures cover qualification assessment, corrective and preventive actions, and complaint handling, supported by 30 qualified service-capable suppliers. The supplier reports 10 production lines, 11–20 quality-control staff, 50 years of combined R&D-engineer experience, ODM and OEM capabilities, SDK availability, and recent new-product development. It supports extensive customization but does not provide 3D software design services. Inventory capability and participation in WHX Labs Dubai 2026 are indicated, while overseas agents or branches, overseas warehouses, and overseas showrooms are absent. Manufacturing subcontracting lacks a valid contract, and no factory environmental impact assessment report is available. Financial records are identified for 2023–2025, but the slices provide no performance values.
Supplier typeThe supplier is identified as a combined company with a business scope covering device sales, second-class medical device sales, instruments and meters, software and hardware, communications equipment, specialized chemicals excluding hazardous chemicals, and industrial automation systems. Its profile also covers manufacturing, export trade, service, quality control, R&D, and sustainability activities, indicating a diversified supplier rather than a narrowly specialized entity.
CertificationsThe supplier reports ISO 13485 and ISO 9001 certifications for supplier management systems, plus ISO 9001:2015, ISO 14001, and ISO 45001:2018-related sustainability certifications. These certifications explicitly support quality, medical-device management, environmental, and occupational-safety systems.
After-Sales capabilityThe supplier has written procedures and implementation records for complaint handling and corrective/preventive actions, and reports 30 qualified suppliers for service capability. It also has inventory capability and has participated in WHX Labs Dubai 2026, but it lacks overseas agents or branches, overseas warehouses, and overseas showrooms; therefore, the documented service processes are positive, while international service infrastructure is limited.
R&D capabilityThe supplier reports 50 years of total R&D-engineer experience, new products developed during the past year, ODM services, and an available SDK. These details provide explicit evidence of active R&D and product-development capability, although 3D software design services are not offered.
Production capacityThe supplier operates 10 production lines, has 11–20 quality-control staff, and reports in-stock service capability. However, the factory and related subcontractors do not have a valid manufacturing-capacity contract, which is a documented weakness in production governance.
Customization capabilityThe supplier offers customization from samples, customization from designs, full customization, minor customization, and flexible customization, and also provides ODM services. This indicates broad product adaptation and original-design support, despite the absence of 3D software design services.
Client casesThe supplier states that its products and services are available throughout the country, provides OEM services for well-known brands, and participated in the WHX Labs Dubai 2026 offline trade show. These are explicit market and customer-related references, but the slices do not identify specific customer names, projects, order histories, or performance outcomes.

Product Q&A

Q:What is the detection limit of the kit?
A:
The kit has a Limit of Detection (LoD) of 12.5 IU/mL.
Q:Which HCV genotypes does the kit cover?
A:
It covers Hepatitis C Virus genotypes 1 through 6.
Q:Can this kit be used for blood screening?
A:
No, this kit should not be used for blood screening.
Q:Is customization available for this product?
A:
Yes, we offer full, minor, and flexible customization from samples or designs.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1.

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