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Realtime PCR Detection Kit Rubella Virus Nucleic Acid Detection Kits
US$3.00
200-399 sets
US$2.50
400-499 sets
US$2.00
500+ sets

Product profile

Customization

Available

Type

IVD Reagent

Product Name

Rubella Virus Detection Kit

Model NO.

BW-RM-Rubella

Sample

Available

Color

Transparent

Appearance

Liquid

MOQ

50 Test

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

Key features

Fluorescence RT-PCR Method: Utilizes specific primers and Taqman probes for accurate Rubella Virus nucleic acid detection.
Internal Control System: Includes internal control primers to monitor sample collection and avoid false negative results.
Broad Instrument Compatibility: Compatible with ABI, Bio-Rad, Agilent, Roche, Cepheid, and Rotor-Gene real-time PCR instruments.
ISO9001 & CE Certified: Manufactured under ISO9001:2015 quality management system with CE certification for export.
ODM and OEM Services: Offers full customization including specification, logo, and packaging based on client requirements.
High Production Capacity: Monthly production capacity of 50,000 tests with 100% finished product inspection.
Flexible MOQ Options: Standard MOQ is 10 boxes; customized products allow negotiated scales for specifications and packing.
Fast Lead Time: Standard lead time is 5-10 days; large orders take 7-15 days or can be negotiated.

Company profile

Hangzhou Beiwo Medical Technology Co., Ltd.
Importers and ExportersPatents AwardedStandardized quality controlR&D Capabilities
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.

Product Q&A

Q:What kinds of products do you have?
A:
We offer sample preparation and purification, analysis and detection, including reagents, instruments, and automation platforms 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.

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