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My-B020ie Fluorescence PCR Nucleic Acid Detection Kit
US$1,650.00
2 BOX
Product profile
Customization
AvailableType
Nucleic Acid Detection KitWeight
70kgModel NO.
MY-B020IEFeature
Fluorescence PCRMOQ
2 BoxTransport Package
96 Test/Box 165box/CTNSpecification
64*67*66cmTrademark
MayamedOrigin
ChinaProduction Capacity
50000PCSKey features
Fluorescence PCR Technology: Uses specific primers and Taqman probes for ORF1ab and N genes to achieve qualitative detection.
Internal Control Monitoring: Includes RNase P mRNA to monitor the extraction and detection process in normal human epithelial cells.
OEM and ODM Services: Offers full customization, minor customization, and flexible customization from samples or designs.
100% Finished Product Inspection: Conducts visual and function inspection on all finished products with uniform instructions.
Fast Lead Time: Peak and off-peak season lead times are both within 15 workdays.
Traceable Raw Materials: Ensures full traceability of all raw materials used in production.
Multiple Payment Options: Accepts LC, T/T, D/P, PayPal, Western Union, and small-amount payments.
Established Manufacturer: Operating since 2011 with 3 production lines and 3 QA/QC inspectors.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 12 years CertifiedNearest Port: Guangzhou Port, Shenzhen PortAverage Response Time: ≤5.94h
AI-Powered supplier vetting
SummaryThe supplier is identified as a Guangzhou-based trading company with a combined company type, rather than explicitly as a manufacturer. It demonstrates broad customization, ODM and OEM capabilities, recent new-product activity, and documented R&D design review, verification, and validation records. Production-related evidence includes three production lines, 50 quality-control staff, inventory capability, contracted associated subcontractors, and lead times within 15 workdays in both peak and off-season periods. Export experience is established at 12 years, with 90% of sales from exports and self-operated import/export rights. However, no certifications, customer cases, overseas warehouses or showrooms, SDK availability, or R&D patents are documented. Financial information is present only as year references, without sufficient evidence to assess credibility.
After-Sales capabilityThe company description states that the team provides comprehensive after-sales service, and overseas service offerings include training. However, the supplier reports no overseas warehouse or showroom and lists zero countries for overseas services, so the scope of international support appears limited.
R&D capabilityThe supplier reports new products within the past year, provides ODM services, and maintains design input, output, review, verification, and validation documents available for audit. It uses PS and CAD, but has no available SDK and reports zero R&D patents, indicating documented development activity but limited evidence of proprietary innovation.
Production capacityThe supplier reports three production lines, 50 quality-control staff, inventory capability, valid contracts with each associated subcontractor, and average lead times within 15 workdays in both peak and off-season. Finished-product inspection follows written instructions uniformly, supporting a positive assessment of operational capacity and process control.
Customization capabilityBoth R&D and design-service records list customization from samples, designs, full customization, minor customization, and flexible customization. The supplier also reports ODM capability, providing explicit evidence of broad customization support.
Client casesThe supplier states that it provides OEM services for well-known brands, which is evidence of brand-related customer experience. No customer names, project details, order history, or verifiable case studies are provided, limiting assessment of the depth and relevance of those cases.
Product Q&A
Q:What is the detection principle?
A:
It uses fluorescence PCR technology with specific primers and Taqman probes for ORF1ab and N genes.
Q:Does the kit include an internal control?
A:
Yes, it uses RNase P mRNA to monitor the extraction and detection process.
Q:What are the customization options?
A:
We offer full customization, minor customization, and flexible customization from samples or designs.
Q:What is the lead time for orders?
A:
Both peak and off-peak season lead times are within 15 workdays.
Q:What payment methods are accepted?
A:
We accept LC, T/T, D/P, PayPal, Western Union, and small-amount payments.
Send Inquiry
*To:
Guangzhou Maya Medical Equipment Co., Ltd.
Guangzhou Maya Medical Equipment Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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