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Singclean Ivd Monkeypox Virus Rapid Diagnostic Test (Fluorescence PCR) 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 SterilizationModel NO.
MonkeypoxQuality 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
Fluorescence PCR Principle: Utilizes advanced fluorescence PCR technology for rapid and accurate detection.
High Specificity: No cross-reaction with measles, rubella, parvovirus B19, varicella, syphilis, or herpes simplex viruses.
Low Detection Limit: Minimum detection limit of 400 copies/mL ensures sensitivity for early diagnosis.
CE Certificate: Product holds CE certification for compliance with European safety standards.
OEM/ODM Service: Full customization available including brand name and packaging options.
High Precision: Coefficient of variation (CV%) for intra-assay precision is less than or equal to 5%.
One Year Warranty: Comes with a one-year quality guarantee period for peace of mind.
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: ≤5.35h
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 detection principle of this test kit?
A:
The kit uses the Fluorescence PCR principle to detect nucleic acid fragments of the monkeypox virus.
Q:What types of specimens can be tested?
A:
It is suitable for serum and human pustular or vesicular rash specimens from suspected individuals.
Q:Is the product customizable?
A:
Yes, full customization is available, including brand name and packaging options.
Q:What is the minimum detection limit?
A:
The kit has a minimum detection limit of 400 copies/mL.
Q:Does the kit have cross-reactions with other viruses?
A:
No, it shows no cross-reaction with measles, rubella, parvovirus B19, varicella zoster, syphilis, or herpes simplex viruses.
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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