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Singclean Monkeypox Virus Antigen Test Kit Rapid Diagnostic Test
US$2.40-2.80
1,000 Pieces

Product profile

Customization

Available

Type

IVD Reagent

Shelf Life

1 Year

Model NO.

singclean

Storage Condition

4° C to 30°c

Transport Package

Box, Carton

Specification

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

Trademark

Singclean

Origin

Hangzhou, China

Production Capacity

50000/Day

Key features

Rapid Monkeypox Detection: Immunochromatographic assay for qualitative detection of Monkeypox virus antigen in human body fluids.
Internal Quality Control: Features an internal control line (C band) to ensure test validity and procedural correctness.
Professional Manufacturer: Produced by Hangzhou Singclean, a top 3 Hyaluronic Acid manufacturer with 20 years of industry expertise.
Full Customization Support: Offers full customization options including OEM and ODM services for tailored product solutions.
Strict Quality Assurance: 100% finished product inspection with 66 QA/QC inspectors ensuring high manufacturing standards.
Flexible Payment Terms: Accepts LC, T/T, D/P, PayPal, Western Union, and small-amount payments for convenient transactions.
Fast Lead Time: Off-season lead time within 15 workdays; peak season lead time approximately one month.

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: ≤5.01h

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 intended use of this test kit?
A:
It is a solid phase immunochromatographic assay for the rapid, qualitative detection of Monkeypox virus antigen in human body fluids. It provides only a preliminary result.
Q:What is the shelf life of the test kit?
A:
The validity period is 24 months. Do not use the test after the expiration date indicated on the package.
Q:What samples can be used for testing?
A:
The test can be performed using human body fluid samples. Samples should be collected in clean containers and brought to room temperature before testing.
Q:How long does it take to get results?
A:
Wait for the colored line to appear. The result should be read in 15 minutes. Do not interpret the result after 20 minutes.
Q:Is customization available for this product?
A:
Yes, full customization options are available, including OEM and ODM services, supported by 22 R&D engineers.

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