Hpv Multiplex Detection Kit Human Papilloma Virus Genotyping Detection Kit 11+3

Name: Hpv Multiplex Detection Kit Human Papilloma Virus Genotyping Detection Kit 11+3
Brand: Hangzhou Beiwo Medical Technology Co., Ltd.
SKU: 2122349305

Zhejiang, ChinaHangzhou Beiwo Medical Technology Co., Ltd.

US$3.00

200-399 sets

US$2.67

400-499 sets

US$2.45

500+ sets

Product profile

Customization

Available

Type

IVD Reagent

Product Name

Hpv DNA Nucleic Acid Detection Kit

Model NO.

RM-FP-069

Sample

Available

Color

Transparent

Appearance

Liquid

MOQ

20 Test

Brand

Runmei

Storage

-20

Package

Box

Certificate

ISO MSDS CE

Transport Package

Cold Chain

Specification

50 test

Trademark

RUNMEI

Origin

Hunan, China

HS Code

3822190090

Production Capacity

5000boxes Per Month

Company profile

Importers and ExportersPatents AwardedStandardized quality controlR&D Capabilities

Hangzhou Beiwo Medical Technology Co., Ltd.

Zhejiang, China

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: ≤0.70h

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.