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Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3
US$3.00
200-399 sets
US$2.67
400-499 sets
US$2.45
500+ sets
Product profile
Customization
AvailableType
IVD ReagentClassification
Biochemical ReagentsModel NO.
RM-FP-069Grade
ArSpecific Usage
for Biological PurposeUsage
Diagnostic ReagentsHabit Appellation
Second Kind of ReagentApplication
Scientific Research, HealthProduct Name
Hpv DNA Nucleic Acid Detection KitSample
AvailableColor
TransparentAppearance
LiquidMOQ
20 TestBrand
RunmeiStorage
-20Certificate
ISO MSDS CETransport Package
Cold ChainSpecification
50 testTrademark
RUNMEIOrigin
Hunan, ChinaHS Code
3822190090Production Capacity
5000boxes Per MonthKey features
Comprehensive HPV Genotyping: Detects 14 HPV types including 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 in parallel.
Fluorescent PCR Technology: Uses Taqman probes and internal controls to ensure accurate detection and avoid false negatives.
Flexible Kit Specifications: Available in 20, 50, and 200 tests per kit to meet varying laboratory needs.
Broad Instrument Compatibility: Compatible with ABI, Bio-Rad, Agilent, Roche, Cepheid, and Rotor-Gene real-time PCR systems.
ISO9001 and CE Certified: Manufactured under ISO9001 quality management system with CE certification for export.
ODM and OEM Services: Customizable specifications, logos, and packaging available for bulk orders.
Fast Production Lead Time: Standard lead time is 5-10 days, with 7-15 days for large volume orders.
High Monthly Capacity: Production capacity reaches 50,000 tests per month to ensure supply stability.
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: 4 Years CertifiedNearest Port: Ningbo, ShanghaiAverage Response Time: ≤0.52h
AI-Powered supplier vetting
SummaryThe supplier is identified as a combined company with business activities covering Class I medical-device production and sales, certain Class II medical-device and cosmetics sales, technical services, and related technology activities. It holds CE and ISO9001:2015 certifications. The supplier demonstrates R&D, ODM, OEM, SDK, customization, and new-product capabilities, including 11 R&D engineers. Service procedures, complaint handling, and corrective/preventive-action procedures are documented and followed. It has inventory capacity and export capability, but no valid manufacturing-capacity contract with related subcontractors, overseas warehouse, or overseas showroom. No cooperation with Fortune 500 companies is reported, while repeat-buyer data is limited to 10%–30%.
Supplier typeThe supplier is classified as a combined company. Its stated scope includes production and sales of Class I medical devices, selected medical-mask and cosmetics activities, technical services and development, instrument sales, and domestic and sales-agent activities. This indicates a diversified business scope, although the information does not identify a more specific organizational or manufacturer classification.
CertificationsThe supplier reports CE product compliance certification and an ISO9001:2015 management-system certificate. These are explicit certifications relevant to product compliance and quality management, although the certified product scope is not specified.
After-Sales capabilityThe supplier has written procedures and followed records for service-capability assessment, corrective and preventive actions, and effective customer-complaint handling. It also reports inventory capacity, but lacks overseas warehouse and overseas showroom services; therefore, documented service processes are a strength while overseas support is limited.
R&D capabilityThe supplier reports new products within the past year, 11 R&D engineers, ODM services, and an available SDK. These explicit capabilities support active product development and technical innovation.
Production capacityThe business scope explicitly includes production of Class I medical devices, and the supplier reports inventory capacity, standardized finished-product inspection instructions, and self-operated import/export rights. However, it also states that neither the factory nor related subcontractors have a valid manufacturing-capacity contract, which is a specific production-governance deficiency.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization. The same range is reported for design services, indicating broad stated customization coverage.
Product Q&A
Q:What kinds of products do you have?
A:
sample preparation and purification, analysis and detection, BEIWO has corresponding reagents, instruments and even automation platform for scientific research institutions, academic institutions and industrial customers in the biopharmaceutical industry.
Q:How can I get the sample to check your quality?
A:
We can ship the sample by international express like FEDEX, DHL etc, or we can choose the appropriate express logistics for you according to your requirements. Sample and freight cost will be needed.
Q:Can you provide different specifications of the kits according to the quantity we need?
A:
Yes, we can provide the kits according your requirements, and we also can do ODM and OEM.
Q:What's your MOQ?
A:
The MOQ for kits is 10 boxes. If some samples are needed, the total number of samples cannot be less than 5 boxes. For customized products, you can set the scales with your specification, logo, packing, etc, so the MOQ shall be negotiated.
Q:Do you have any certificates?
A:
Yes, we have the certificatesISO9001, CErequired for export and local import custom clearance.
Send Inquiry
*To:
Hangzhou Beiwo Medical Technology Co., Ltd.
Hangzhou Beiwo Medical Technology Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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