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Singclean Monkeypox Virus Nucleic Acid Detection Kit (Fluorescence PCR) Diagnostic Test with CE Certificate
US$0.30-3.80
1,000 Pieces
Sample price:US$3.00/piece.Request sample
Product profile
Customization
AvailableType
IVD Reagent, Ivd ReagentEthylene Oxide Sterilization
Without Ethylene Oxide SterilizationQuality Guarantee Period
One YearGroup
AdultLogo Printing
Without Logo PrintingMaterial
Cassette/Panel/CupCertificates
ISO13485/CE/CfdaPrinciple
Fluorescence PCRSpecimen
Blood/PusForm
CupBrand Name
Singclean/Other BrandStorage
-25 Degrees CelsiusTransport Package
CartonsSpecification
25 tests/kit, 50 tests/kitTrademark
Singclean/OEMOrigin
ChinaHS Code
3302100090Production Capacity
5000/DayKey features
High Sensitivity Detection: Minimum detection limit of 400 copies/mL for accurate results.
CE Certified Quality: Obtained CE and ISO13485 certificates for reliable diagnostic performance.
High Specificity: No cross-reaction with measles, rubella, syphilis, or herpes simplex viruses.
Fast Turnaround Time: Suitable for rapid diagnosis of monkeypox virus infection in suspected cases.
Flexible Packaging Options: Available in 25 tests/kit and 50 tests/kit configurations.
Comprehensive Support: OEM and ODM services available with full customization options.
Robust QA/QC: 100% finished product inspection by 66 dedicated QA/QC inspectors.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Full Customization CertifiedExport Year: Shanghai Port CertifiedNearest Port: Shanghai PortAverage Response Time: ≤3.78h
AI-Powered supplier vetting
SummaryThe supplier is identified as a manufacturing factory in Hangzhou’s Qiantang District, with a business scope covering medical devices, cosmetics, masks, disinfectants, technical services, and import/export activities. It reports ISO 9001:2015 and CE certifications, 100% finished-product inspection, 58 quality assurance and control inspectors, and documented corrective-action and complaint-handling procedures. Manufacturing contracts with associated subcontractors are in place, and the supplier offers OEM, ODM, and broad customization services. However, it reports no in-stock capacity, overseas warehouse, overseas showroom, overseas agents or branches, or SDK availability. No new product was developed in the past year, and the company did not conduct regular fire drills during that period. Customer-case evidence is limited to OEM service for well-known brands and participation in one offline trade event.
Supplier typeThe supplier is explicitly identified as a factory, with associated companies in manufacturing. Its registered business scope includes first-category medical device production, second-category medical device sales, cosmetics, masks, disinfectants, technical services, and import/export activities.
CertificationsThe supplier reports an ISO 9001:2015 management-system certificate and CE certification for products. It also states that quality assurance exists and that quality-control processes are supported by documented procedures and records.
R&D capabilityThe supplier reports no available SDK and no new products during the past year, which are explicit limitations for software-enabled and recent product innovation. It does provide ODM services, but the available evidence does not establish strong ongoing innovation capability.
Production capacityThe supplier is a manufacturing factory with 100% finished-product inspection, 58 quality assurance and control inspectors, listed mixing, filling, sterilizing, and packing equipment, and a reported peak-season fulfillment time of one month. Valid manufacturing contracts with associated subcontractors are in place, although the supplier has no in-stock capacity.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, and full customization. It also provides ODM services and reports OEM capability for well-known brands, while its own-brand product quality-control capability covers Singclean and Singjoint.
Product Q&A
Q:What is the minimum detection limit of the kit?
A:
The kit has a minimum detection limit of 400 copies/mL.
Q:Does the kit cross-react with other viruses?
A:
No, the kit shows no cross-reaction with measles, rubella, parvovirus B19, varicella zoster, syphilis, or herpes simplex viruses.
Q:Is OEM or ODM service available?
A:
Yes, OEM and ODM services are available with full customization options.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 10 PCS.
Q:What certificates does the product have?
A:
The product holds CE, ISO13485, and Cfda certificates.
Send Inquiry
*To:
Hangzhou Singclean Medical Products Co., Ltd.
Hangzhou Singclean Medical Products Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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