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Ivd Reagent Singclean Medical Products Rapid Diagnostic Monkeypox Virus Test with Low Price
US$2.50-2.90
1,000 Pieces

Product profile

Customization

Available

Type

IVD Reagent

Shelf Life

1 Year

Storage Condition

4° C to 30°c

Transport Package

Box, Carton

Specification

1test/box, 5tests/box, 20 tests/box

Trademark

Singclean

Origin

Hangzhou, China

Production Capacity

50000/Day

Key features

Rapid Monkeypox Detection: Detects IgG/IgM antibodies in human blood using immunochromatography for quick qualitative results.
High Accuracy & Control: Features internal quality control line (C) to ensure valid chromatographic process and sample volume.
Flexible Packaging Options: Available in 1, 5, or 20 tests per box to suit different laboratory or clinical needs.
CE Certified Quality: Product holds CE certification, ensuring compliance with European health and safety standards.
Full Customization Support: Offers full customization options including OEM and ODM services for tailored product solutions.
Manufacturer Direct Supply: Direct from factory with 546 employees, 10 production lines, and 66 QA/QC inspectors.
Comprehensive Testing Kit: Includes test cassette, desiccant, dropper, buffer, and package insert for immediate use.

Company profile

Hangzhou Singclean Medical Products Co., Ltd.
Importers and ExportersExhibition Experience
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: ≤3.77h

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 does the Monkeypox test detect?
A:
It is a qualitative assay for the rapid detection of IgG and IgM antibodies to Monkeypox virus in human blood.
Q:What is the shelf life after opening?
A:
After the foil bag is opened, the validity period is 1 hour. Best results are obtained if used within this time.
Q:What samples can be used for testing?
A:
The test can be performed using Serum, Plasma, or Whole Blood specimens.
Q:How long should I wait for results?
A:
Read the result at 10 minutes. Do not interpret the result after 15 minutes.
Q:Is this test for self-diagnosis?
A:
No, it provides only a preliminary result. Reactive specimens must be confirmed with alternative testing methods and clinical findings.

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