Ivd Reagent Singclean Diagnostic Monkeypox Virus with Good Price CE
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Product Highlights
- Rapid Qualitative Detection: Detects IgG/IgM antibodies to Monkeypox virus in human blood using immunochromatography.
- CE Certified Product: Meets European safety and quality standards for in vitro diagnostic reagents.
- Full Customization Available: Offers full customization options for packaging and product specifications.
- Complete Test Kit Components: Includes test cassette, desiccant, dropper, buffer, and package insert.
- Dual Antibody Detection: Simultaneously detects IgM and IgG antibodies for comprehensive screening.
- ISO 9001:2015 Certified: Manufacturer holds ISO9001:2015 certification for quality management systems.
- OEM and ODM Services: Provides both OEM and ODM services for customized production needs.
Product Attributes
- 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
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Product Description
Singclean Monkeypox virus lgG/IgM Test Kit(Immunochromatography)
Key Words: Hyaluronic Acid, dermal filler, facial hyaluronate acid, cosmetic products, plastic surgery, high quality, good effect, Anti Aging, Nasolabial folds, lip filler
PACKAGING SPECIFICATIONS
1 test/box, 5 tests/box, 20 tests/box
MATERIALS SUPPLIED
Each sealed pouches contains a test cassette, a desiccant, a dropper, Buffer, Package insert
Intended Use
Monkeypox virus IgG/IgM Test Kit (lmmunochromatography) is a solid phase immunochromatographic assay for the rapid, qualitative detection of lgG/IgM antibody to Monkeypox virus in human blood.This test provides only apreliminary test result. Therefore, any reactive specimen with the Monkeypox virus lgG/IgM Test Kit (lmmunochro-matography) must be confirmed with alternative testing method(s) and clinical findings.
Introduction
Monkeypox is a viral zoonosis (a virus transmitted to humans from animals) with symptoms very similar to those seen in the past in smallpox patients, although it is clinically less severe. With the eradication of smallpox in 1980 and subsequent cessation of smallpox vaccination, monkeypox has emerged as the most important orthopoxvirus for public health. Monkeypox primarily occurs in Central and West Africa, often in proximity to tropical rainforests and has been increasingly appearing in urban areas. Animal hosts include a range of rodents and non-human primates.
Principle
Monkeypox vius lgG/IgM Test kit (lmmunochromatography) uses the principle of immuno-chromatography. The test uses anti-human lgM antibody (test line lgM), ant-human lgG (test line lgG) and goat anti-mouse lgG(control line C) immobilised on a nitrocellulose membrane. The conjugate pad contains microsphere conjugated to recombinant Mankeypox antigens conjugated with microsphere.When a specimen followed by assay buffer is added to the sample well, IgM &/or lgG antibodies if present, will bind to Monkeypox conjugates making antigen antibodies complex. This complex migrates through nitrocellulose membrane by capillary action.When the complex meets theline of the corresponding immcbilized antibody (anti-human IgM&/or anit-human lgG) the complex is trapped forming a band which confirm a reactive test result.
Regardless of the presence of Monkeypox lgG/gM antibody in the test sample, a colored band will appear on thequality control line (line C). The colored band appearing on the quality control line (line C) is used to determinewhether there are enough samples and whether the chromatographic process meets the nomal standard, and alsoserves as the internal control standard of the reagent.
STORAGE CONDITIONS AND VALIDITY PERIOD
The test kit should be stored in a sealed aluminum foil bag at 4ºC ~30ºCC, and the validity period is 24 months. Afterthe foil bag is opened, the validity period is 1 hour.
TEST METHOD
Allow test cassette, specimen, buffer and/or controls to equilibrate to room temperature prior to testing.
1.Remove the test cassette from the sealed foil pouch and use it as soon as possible. Best results will be obtainedif the assay is performed within one hour.
2.Place the test device on a clean and level surface.
For Serum or Plasma Specimens:
With the provided dropper, draw serum/plasma specimen and then add 1 drop serumplasma specimen into thesample well(S).Then add 2 drops of buffer to the sample well(S) immediately. Avoid air bubbles.
For Whole Blood Specimen:
With the provided dropper and transfer 1 drop of whole blood to the sample well(S) of the test device, then add 2 drops of buffer to the sample well(S) immediately. Avoid air bubbles.
Wait for the colored line(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 15 minutes.
INTERPRETATION OF RESULTS
NEGATIVE: lf only the C band is present, the absence of any burgundy color in the both T bands (lgG and lgM)indicates that no anti-Monkeypox antibodies are detected in the specimen.The result is negative.
lgM POSITIVE:
ln addition to the presence of C band, if only lgM band is developed, the test indicates for the presence of lgM anti-Monkeypox in the specimen.The result is lgM anti-Monkeypox positive.
lgG POSITIVE:
ln addition to the presence of C band, if only lgG band is developed, the test indicates for the presence of lgG anti-Monkeypox in the specimen. The result is lgG anti-Monkeypox positive.
About the Supplier
This supplier has been audited by BV. Verify the report on the official BV website with ID "MIC-ASR2532126". Items marked "" are certified.
Company Profile
Company Introduction
Hangzhou Singclean Medical Products Co., Ltd., established in March 2002 with registered capital of 80, 000, 000 RMB, is a national high and new technology enterprise integrating the R&D, production and sales of medical biomaterials.With highly-qualified staff, thorough quality management system and first-class facilities, the company ensures the continuous production of medical devices and drug injection products of Class III that conform to the laws and regulations of National Medical Products Administration (NMPA) and EU MDR.
Cooperation
The company set up a joint research center with Zhejiang University of Science and Technology, and has well established R&D cooperation relations with Zhejiang University, Donghua University and Zhejiang University of Technology, developing four series of new products with proprietary intellectual property rights, and with a variety of high-tech products to be developed cooperatively.The company also built an R & D platform for medical biomaterials that keeps up with the international level, and made major breakthrough in many key technologies such as those for stopping bleeding, anti-adhesion, and tissue engineering basic materials, with more than 55 patents obtained and a number of products applying for the patents.
Our manufacturing
The company's plant in Xiasha covers the construction area of 174014.83 m²And producing tract of 13, 200 m²Including cleanrooms of 2, 300 m²In which cleanroom of Class C covers 2, 000 m²And that of Class B covers 300 m²With over 60 m²Of which follows into Class A.A new cleanroom up to GMP standard was set up in this plant, and the Pharmaceutical Production License was obtained in 2012.It will produce all kinds of medical equipment and medical 10 million sets, production value 2 billion, In addition, the plant has introduced more production facilities such as the Invoa filling machine from Germany, the sterilizer from GETINGE, the semi-automatic filling and sealing equipment from Pluemat, 5T / h purified water machine, 3T / h water for injection machine, and 1T / h of pure steam generator.
Quality system
Respect for life strict quality control
The company has set up a documentation-based GB/T19001-2008, YY/T0287-2003, Good manufacturing Practice for medical devices, Good manufacturing practice for In vitro diagnostic reagents, good manufacturing practice of drug, 2010, medical device directive (MDD93/42/EEC ), according to quality objectives, auit resullt, data analysis, corrective and preventive actions and management review, in order to maitain the continued suitability and effectivenss of the quality managenment system.
Technological Innovation
Cohesion of technological strength improving core competitiveness
The company has been always laid stress on product rsearch and development, investing annually 10% of the sales to comstruction of R&D center, new product development and introduction of advance equipments.The R&D center is equipped with cleanroom in Class 10000(including Class 100) of more than 200m², and it has acquired a number of patent technologies.
Product center
Committing herself to develop new types of composite and smart biomaterials, the company majors in producing biodegradable bio-materials and their derivatives, and has at present products of 8 series (chitosan, medical sodium hyaluronate gels, cross-linked hyaluronic acidsodium gels, microporous polysaccharide, oxidized regenerated cellulose, basic materials of tissue engineering, in vitro diagnostic reagents), 50 varieties of cosmetics are being exported to more than 120 countries around the world, such as:Italy, Russia, Turkey, France, Brazil, Chile, Australia, and Canada.Until now, Singclean has got 30+ CE certificates, 16 medical device registration certificates and 46 patent certificates.At Singclean, all their 600 employees are working with the best and committed to excellence.
About Our Factory & Business Background
-
Business Type
- Manufacturer/Factory & Trading Company
- Address
- No. 125(E), 10th Street, Hangzhou Qiantang Area, China 310018, Hangzhou, Zhejiang, China
-
Plant Area
- 13045 square meters
-
Number of Employees
- 546
-
Registered Capital
- 80,000,000 RMB
-
Terms of Payment
- LC, T/T, D/P, PayPal, Western Union, Small-amount payment
-
International Commercial Terms(Incoterms)
- FOB, CIF, CFR, EXW
-
Average Lead Time
-
Peak Season Lead Time: one month
Off Season Lead Time: within 15 workdays -
Nearest Port
- Shanghai Port
-
Minimum Order Quantity
- 10 PCS
-
Supply Chain Partners
- 260
Our Production Capability & Technical Expertise
-
Main Products
- Dermal Filler, Joint Lubrication for Knee, Cross-Linked Sodium Hyaluronate Gels, Absorbable Hemostatic Particles, Oxidized Regenerated Cellulose, Poly-L-Lactic Acid Filler For Injection
-
Production Lines
- 10
-
Production Machines
- Testing Machine
-
QA/QC inspectors
- 66 people
-
Inspection Type for Finished Products
- 100% inspection(Visual inspection & Function inspection)
-
Inspection Method for Finished Products
- Finished product checked by packing staff
-
Customization Options
- Full Customization
-
ODM Service Available
- Yes
-
OEM Service Available
- Yes
-
R&D Engineers
- 22 people
-
Traceability of Raw Materials
- Yes
Our Industry Experience & Global Business Record
-
Year of Establishment
- 2003-03-25
-
Export Year
- Shanghai Port
-
Main Markets
- North America, Europe, Southeast Asia/ Mideast, Africa, Australia, Domestic
-
Repeat Buyers Choice
- 50%~80%
-
Number of Foreign Trading Staff
- 54
-
Overseas Agent/Branch
- Yes
-
New Products Launched in Last year
- Yes
Our Certifications, Standards & Industry Recognition
-
Management System Certification
- ISO9001:2015, Others
-
Product Certification
- CE
-
Cooperated with Fortune 500
- No
FAQ
- What samples can be tested with this kit?
- This kit is designed for the detection of antibodies in human blood, including serum, plasma, and whole blood specimens.
- How long does it take to get results?
- Results should be read at 10 minutes. Do not interpret results after 15 minutes.
- Is this a definitive diagnostic test?
- No, this provides only a preliminary result. Any reactive specimen must be confirmed with alternative testing methods and clinical findings.
- What is the minimum order quantity?
- The minimum order quantity is 10 pieces.
- Do you offer customization services?
- Yes, we offer full customization, including OEM and ODM services.
- What are the payment terms?
- We accept LC, T/T, D/P, PayPal, Western Union, and small-amount payments.
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