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The Test Kit, Influenza A&B Sofia is a fluorescent immunoassay system for point‑of‑care detection of influenza A and B antigens. Each unit comprises twenty‑five individual tests and the kits are packed twelve per case, giving a total of three hundred assays per case. The reagents contain monoclonal antibodies conjugated with a fluorescent dye and are supplied by Quidel under product number 20218. The kits require cold‑chain storage at 2‑8 °C and are intended for professional use in clinical laboratories or hospitals.
Fluorescent immunoassays such as Sofia deliver results typically within fifteen minutes and are valued for their quantitative fluorescence signal. In the IVD market, comparable influenza rapid tests are commonly stored between 2 and 8 °C and have a shelf life of about twelve months when unopened. The format of twenty‑five tests per unit aligns with standard batch‑testing workflows in high‑volume diagnostic settings. Typical quality standards for these devices include ISO 13485 compliance and assay sensitivity and specificity each above ninety‑five percent.
Healthcare providers, public‑health agencies and large hospital networks purchase these kits for seasonal flu screening programmes. Importers should request the case dimensions, weight and confirm Incoterms such as FOB or CIF before placing an order. Minimum order quantities are not disclosed in the listing and should be clarified with USA Med Premium. Payment terms, lead times and any required certifications, for example FDA clearance, must be verified directly with the supplier.
| Material | Immunological reagents with monoclonal antibodies and fluorescent dye conjugates |
| Tests per unit | 25 |
| Kits per case | 12 |
| Manufacturer | Quidel |
| Product number | 20218 |
| Storage temperature (typical) | 2‑8 °C |
| Shelf life (typical) | 12 months |
| Result time (typical) | ≈15 minutes |
| Sensitivity (typical) | ≥95 % |
| Specificity (typical) | ≥95 % |
USA Med Premium is listed with a harbor trust tier and operates from 21068 Sheridan St, Fort Lauderdale, Florida 33332, United States. The company’s profile provides a verified address but does not include response‑rate data, indicating that recent communication metrics are unavailable. As a supplier of immunological reagents, USA Med Premium focuses on point‑of‑care diagnostic kits for clinical environments. The listing does not disclose manufacturing capacity, years in operation or client references.
The product offering highlighted in this listing is the Quidel Sofia Influenza A&B rapid test kit, which the supplier distributes under the stated product number. No additional certifications, such as ISO 13485 or CE marking, are explicitly claimed by USA Med Premium in the profile, so buyers should request supporting documentation. The company’s catalogue appears limited to this influenza assay, and any bulk‑order arrangements or custom formulations would need direct negotiation. All other details beyond those provided are absent from the public listing.
This Quidel Sofia Influenza A&B Rapid Test Kit is a fluorescent immunoassay system designed for point-of-care detection of influenza A and B antigens, providing reliable results in minutes. Suitable for clinical laboratories, hospitals, and healthcare facilities conducting flu screening programs. Each kit contains 25 tests per unit, with 12 kits per case, ideal for high-volume diagnostic testing needs. These IVD kits require cold chain storage and are intended for professional use in diagnostic and clinical settings.
| Business Type | Supplier |
| Year Established | Recently Joined |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| Response Time | Contact Supplier |
| Response Rate | New Supplier |
Before placing an order with USA Med Premium, importers should verify the supplier’s harbor trust tier, request a copy of the FDA clearance for the Quidel Sofia kit, and confirm that the product is stored and shipped under cold‑chain conditions. It is advisable to obtain a detailed specification sheet that lists batch numbers, expiry dates and temperature monitoring logs. Any deviation from the listed storage requirements should be clarified to avoid assay degradation.
Logistical arrangements typically involve sea or air freight, with the choice of Incoterm (FOB, CIF or DAP) to be agreed during negotiation. Buyers need to confirm the lead time for case preparation, which is not disclosed in the listing, and request the gross weight and volume per case for accurate freight costing. Customs documentation, including a commercial invoice and certificate of origin, should be prepared in advance to prevent clearance delays.
Upon receipt, importers should perform a visual inspection of case seals and verify temperature loggers to ensure cold‑chain integrity. A functional check of a sample test from each batch can confirm assay performance before distribution to end‑users. Request the manufacturer’s certificate of analysis, ISO 13485 certificate and any additional quality audit reports to complete the due‑diligence process.
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When sourcing Test Kit, Influenza A&B Sofia for your business, securing the right balance of quality and cost is essential. USA Med Premium, a verified supplier based in United States, offers this product with key specifications including Rapid Influenza A&B Antigen Detection Kit, Fluorescent Immunoassay (FIA), and 25 Tests/Kit, 12 Kits/Case. By purchasing directly from the manufacturer or authorized exporter, buyers can negotiate favorable FOB prices starting at $385/Bags and manage bulk orders with a minimum order quantity (MOQ) of 1 Bags. This product is actively traded under HS Code 3822.00.90, making it a staple in the Diagnostic Kits sector with strong demand from importing countries worldwide.
Importing Test Kit, Influenza A&B S requires careful attention to shipping logistics, customs compliance, and secure payment terms. USA Med Premium offers flexible shipping options such as Full Container Load (FCL) or Less than Container Load (LCL) via sea freight. To ensure a smooth transaction, buyers should verify import duties for HS Code 3822.00.90 in their destination country. Common payment methods for international B2B transactions include Letter of Credit (L/C), Telegraphic Transfer (T/T), and Documents against Payment (D/P). All transactions and RFQs are facilitated through EximNext, a leading B2B marketplace designed to make cross-border trade secure and efficient.
Finding trustworthy partners is the foundation of successful importing. The supplier of this Test Kit, Influenza A&B S has been verified on our platform. Whether you are a distributor, wholesaler, or procurement manager, you can request a free quotation, ask for product samples, and finalize your bulk purchase with confidence. EximNext hosts thousands of verified manufacturers and exporters across 200+ countries. Explore similar products in the Diagnostic Kits category and connect with top-tier exporters on our comprehensive global B2B marketplace. Start your sourcing journey today.
Importing Test Kit, Influenza A&B S requires careful attention to shipping logistics, customs compliance, and secure payment terms. Common shipping options include Full Container Load (FCL) or Less than Container Load (LCL) via sea freight. Buyers should verify import duties for HS Code 3822.00.90 in their destination country. Common payment methods include Letter of Credit (L/C), Telegraphic Transfer (T/T), and Documents against Payment (D/P).
The current listed wholesale price for Test Kit, Influenza A&B Sofia from USA Med Premium is $385/Bags on FOB terms from United States. Prices may vary depending on order volume, packaging, and destination. For the most accurate bulk quote, send a direct RFQ to USA Med Premium through EximNext.
The supplier, USA Med Premium, has set a Minimum Order Quantity (MOQ) of 1 Bags for Test Kit, Influenza A&B S. For sample requests or smaller trial orders, contact the supplier directly through our platform's inquiry system.
For international shipping and customs clearance, Test Kit, Influenza A&B Sofia is classified under HS Code 3822.00.90. Buyers should verify their local customs regulations to determine applicable import duties and taxes for this classification.
To import Test Kit, Influenza A&B S from United States, negotiate shipping terms (FOB, CIF, or EXW) directly with USA Med Premium. Ensure you have the necessary import licenses for Diagnostic Kits products in your destination country.
Yes, USA Med Premium is a verified supplier on EximNext. You can view their complete company profile, business registration details, certifications, and export history before placing a bulk order.
The key specifications for Test Kit, Influenza A&B Sofia supplied by USA Med Premium include Rapid Influenza A&B Antigen Detection Kit, Fluorescent Immunoassay (FIA), and 25 Tests/Kit, 12 Kits/Case. For a complete technical data sheet or Certificate of Analysis (COA), send an inquiry directly to the supplier through EximNext.
USA Med Premium offers Test Kit, Influenza A&B S with standard export packaging. Custom packaging, private labeling, and OEM/ODM options may also be available for large wholesale orders.
Test Kit, Influenza A&B S is actively imported by buyers worldwide. Request a destination-specific CIF or CFR quote from USA Med Premium through our platform.
USA Med Premium maintains international quality certifications. These ensure that the Test Kit, Influenza A&B S meets international quality, safety, and regulatory standards required for cross-border trade.
Click "Request Quotation" on this product page, specify your required quantity, preferred shipping terms, and destination country. USA Med Premium will respond with a detailed wholesale quote including FOB pricing, lead time, and payment options.
Common payment methods include Letter of Credit (L/C), Telegraphic Transfer (T/T), Documents against Payment (D/P), and Escrow services. Confirm accepted terms directly with USA Med Premium.
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