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Real Time PCR Human Papilloma Virus Diagnostic Kit Hpv DNA Detection Kit
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-070Usage
Laboratory Reagents, Diagnostic ReagentsHabit Appellation
Second Kind of ReagentApplication
Scientific Research, Health, Research ReagentProperty
Biochemical ReagentSource
Self-Prepared SolutionsOther Names
Human Papilloma Virus Nucleic Acid Detection KitSample
AvailableAppearance
LiquidMOQ
20 TestBrand
RunmeiStorage
-20Product Name
Human Papilloma Virus Nucleic Acid Detection KitPackage
BoxCertificate
ISO MSDS CETransport Package
Cold ChainSpecification
50 testTrademark
RUNMEIOrigin
Hunan, ChinaHS Code
3822190090Production Capacity
5000boxes Per MonthCompany 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.
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*To:
Hangzhou Beiwo Medical Technology Co., Ltd.
Hangzhou Beiwo Medical Technology Co., Ltd.*Content:
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