What are the available kit specifications?

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

Is the product sterilized?

Yes, the product is sterilized using Ethylene Oxide.

What is the warranty period for this product?

The quality guarantee period is two years.

2022 CE Approved MPV PCR Test Kit for Monkeypox Virus

Name: 2022 CE Approved MPV PCR Test Kit for Monkeypox Virus
Brand: Changsha Renji Medical Equipments Co., Ltd.
SKU: 1913561446

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 Time: Completes extraction to amplification in minimum 45 minutes.

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

Multiple Specifications: Available in 50 tests/kit and 200 tests/kit to meet different demands.

Wide Instrument Compatibility: Works with MA-6000, ABI, Bio-Rad, Roche, Cepheid, and Rotor-Gene systems.

CE Approved: Product holds 2022 CE approval for quality and safety compliance.

Ethylene Oxide Sterilization: Sterilized using Ethylene Oxide for safe medical use.

Two-Year Warranty: Comes with a two-year quality guarantee period.

Custom Logo Printing: Supports logo printing services for branding customization.

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.