How long is the quality guarantee period?

The quality guarantee period is two years.

Is the product sterilized?

Yes, the product undergoes Ethylene Oxide Sterilization.

Can I customize the logo on the kit?

Yes, logo printing is available for the test kits.

High Accuracy Monkeypox Detection Kit Reagent PCR Test Monkeypox Rapid Test Kit

Name: High Accuracy Monkeypox Detection Kit Reagent PCR Test Monkeypox Rapid Test Kit
Brand: Changsha Renji Medical Equipments Co., Ltd.
SKU: 1914361816

Hunan, ChinaChangsha Renji Medical Equipments Co., Ltd.

US$3.00

10,000-99,999 Pieces

US$2.50

100,000+ Pieces

Sample price:US$0.00/piece.Request sample

Product profile

Customization

Available

Type

Test Strips & Test Tube

Material

Plastic

Ethylene Oxide Sterilization

Quality Guarantee Period

Two Years

Group

Adult

Logo Printing

With Logo Printing

Nucleic Acid Type

DNA

Species

Virus

Lod

200 Copies/Ml

Transport Package

Carton, 50test/Box 200test/Box

Trademark

Renji

Origin

China

HS Code

3926909090

Production Capacity

500000 PCS / Day

Key features

Rapid Detection: Completes the entire process from extraction to amplification within a minimum of 45 minutes.

High Sensitivity: Assay sensitivity reaches 200 copies/mL for accurate detection.

Flexible Specifications: Available in 50 tests/kit and 200 tests/kit to fulfill different demands.

Broad Compatibility: Compatible with MA-6000, ABI, Bio-Rad, Roche, Cepheid, and Rotor-Gene series instruments.

Two-Year Warranty: Quality guarantee period covers two years for all kits.

Ethylene Oxide Sterilization: Products are sterilized using Ethylene Oxide for safety.

Logo Printing Service: Customized logo printing is available for the test kits.

Versatile Specimen Types: Detects MPV DNA in serum, plasma, vesicular fluid, or pustular lesion fluid.

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 minimum time required for the test?

The entire process from extraction to amplification is completed within a minimum of 45 minutes.

Q:What is the sensitivity of the assay?

The assay sensitivity is 200 copies/mL.

Q:What types of specimens can be tested?

The kit can detect MPV DNA in serum, plasma, vesicular fluid, or pustular lesion fluid.

Q:What are the available kit specifications?

The kit is available in 50 tests/kit and 200 tests/kit specifications.

Q:Which instruments are compatible with this kit?

It works with MA-6000, ABI series, Bio-Rad series, Roche LightCycler R480, Cepheid SmartCycler, Rotor-Gene series, and other multi-channel real-time quantitative PCR instruments.