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Wholesale MPV Detection Kit (PCR Fluorescence Probing) for Monkeypox Virus
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
AvailableType
IVD ReagentNucleic Acid Type
DNAModel NO.
mpv01Species
VirusStorage Temperature
Store at -20°cLod
200 Copies/MlTransport Package
50test/Box 200test/BoxTrademark
RenjiOrigin
ChinaHS Code
3005909000Production Capacity
500000/DayKey features
Rapid Detection Time: Completes extraction to amplification in minimum 45 minutes.
High Sensitivity: Assay sensitivity reaches 200 copies/mL for accurate results.
Flexible Specifications: Available in 50 tests/kit and 200 tests/kit options.
Broad Instrument Compatibility: Works with ABI, Bio-Rad, Roche, Cepheid, and Rotor-Gene systems.
High Specificity: Targets conserved MPV regions using real-time PCR fluorescence.
Diverse Specimen Support: Detects MPV in serum, plasma, and lesion fluid samples.
CE and ISO Certified: Products approved by CE, SGS, and ISO standards.
Direct Manufacturer Supply: Produced by Changsha Renji Medical Equipment Co., Ltd.
Company profile
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 detection limit of the kit?
A:
The kit has an assay sensitivity of 200 copies/mL.
Q:How long does the detection process take?
A:
The entire process from extraction to amplification takes a minimum of 45 minutes.
Q:What types of specimens can be tested?
A:
It detects MPV in serum, plasma, vesicular fluid, and pustular lesion fluid.
Q:Which PCR instruments are compatible with this kit?
A:
Compatible with MA-6000, ABI series, Bio-Rad series, Roche LightCycler R480, Cepheid SmartCycler, and Rotor-Gene series.
Q:What are the available kit specifications?
A:
The kit is available in 50 tests/kit and 200 tests/kit specifications.
Send Inquiry
*To:
Changsha Renji Medical Equipments Co., Ltd.
Changsha Renji Medical Equipments Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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