Is OEM/ODM service available?

Yes, we support OEM/ODM services, including logo printing and custom transport media.

What is the minimum order quantity (MOQ)?

The MOQ is 1,000 pieces, which equals 1 carton.

Professionals Virus Antigen Rapid Test Kit (Colloidal gold method)

Name: Professionals Virus Antigen Rapid Test Kit (Colloidal gold method)
Brand: Changsha Renji Medical Equipments Co., Ltd.
SKU: 1941133952

Hunan, ChinaChangsha Renji Medical Equipments Co., Ltd.

US$1.29

1,000-9,999 Sets

US$1.09

10,000-49,999 Sets

US$0.99

50,000-99,999 Sets

US$0.89

100,000+ Sets

Sample price:US$0.00/piece.Request sample

Product profile

Customization

Available

Type

Test Strips & Test Tube

Material

Plastic

Model NO.

RJ-C-1001

Quality Guarantee Period

Two Years

Group

Adult & Children

Logo Printing

With Logo Printing

Transport Package

Carton

Specification

22.5*14.5*16.5cm

Trademark

Renji

Origin

China

HS Code

3822190020

Production Capacity

100000

Key features

High Accuracy Rate: Provides over 95% accuracy for qualitative detection of nucleoprotein in saliva.

Fast Result Time: Delivers preliminary test results within 15-20 minutes for rapid diagnosis.

Professional Grade: Designed for use by healthcare professionals to aid in infection diagnosis.

CE & ISO Certified: Complies with CE, ISO 13485, and ISO 9001 standards for quality assurance.

OEM/ODM Support: Offers customization services including logo printing and transport media.

Flexible MOQ: Low minimum order quantity of 1,000 pieces (1 carton) for easy entry.

Free Samples: Free samples are available now for evaluation before bulk ordering.

Company profile

Self-brandedStandardized quality controlR&D CapabilitiesManagement Certification

Changsha Renji Medical Equipments Co., Ltd.

Hunan, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2020-10-01Nearest Port: guangzhou, shenzhen, shanghaiAverage Response Time: ≤6.78hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF, FCA, EXW

AI-Powered supplier vetting

SummaryThe supplier is identified as a manufacturing factory producing sanitary materials, medical supplies, medical devices, disinfection products, and sanitary equipment. It reports customization from samples, designs, and full specifications, with two production lines and export markets spanning multiple regions. Quality and service procedures are documented, and the supplier states that it holds or has products approved by CE, SGS, ISO13485, NMPA, and ISO9001:2015-related certification. It also reports OEM service for known brands and experience exporting to more than 50 countries. However, no SDK is available, and the supplier lacks in-stock service, overseas warehouse, overseas showroom, and a valid manufacturing-capacity contract with affiliated subcontractors. Financial information is represented only by years rather than usable performance figures, so financial credibility cannot be determined.

Supplier typeThe supplier is explicitly identified as a factory, with a business scope covering manufacturing of sanitary materials, medical supplies, medical devices, disinfection products, and sanitary equipment. Its associated companies are classified in manufacturing, supporting a direct manufacturing-supplier profile.

CertificationsThe supplier reports an ISO9001:2015 certificate and states that its products have been approved by CE, SGS, ISO13485, and NMPA, among others. These stated certifications and approvals provide explicit evidence of certification coverage, although the slices do not provide certificate numbers, validity dates, or scope details.

After-Sales capabilityThe supplier reports written and followed procedures for service-capability assessment, corrective and preventive actions, and customer complaint handling. This is explicit evidence of a documented after-sales and complaint-management system.

R&D capabilityThe supplier explicitly reports no available SDK, which limits evidence of software-development or integration capability. Although it emphasizes product certifications and customer-oriented management, the slices do not establish broader research, product-development, or innovation performance.

Production capacityThe supplier operates two production lines, reports peak-season fulfillment of one month and off-peak lead time within 15 working days, and has export access through major Chinese ports. However, it reports no in-stock capacity and no valid manufacturing-capacity contract with affiliated subcontractors, creating explicit operational limitations despite its stated factory capacity.

Customization capabilityThe supplier explicitly offers customization from samples, designs, and full customization, and also reports OEM service for known brands. These capabilities directly support customized and OEM manufacturing requirements.

Client casesThe supplier states that it provides OEM services for known brands and has export experience involving more than 50 countries. These statements indicate brand-related and international customer experience, but no specific customer names, project details, or independently verifiable cases are provided.

Product Q&A

Q:What is the intended use of this kit?

It is a lateral flow immunoassay for the qualitative detection of nucleoprotein in saliva, intended for use by professionals to aid in the diagnosis of infection.

Q:How long does it take to get results?

The result time is 15-20 minutes, providing a quick preliminary test result.

Q:What is the accuracy of the test?

The accuracy is over 95%.

Q:What is the validity period of the kit?

The validity period is 24 months.

Q:What certifications does the product have?

The product holds CE, ISO 13485, and ISO 9001 certifications.