HS 382212 For Zika and other diseases transmitted by mosquitoes of the genus Aedes
Quick Answer: Diagnostic reagents for Zika and other mosquito-borne diseases, specifically those transmitted by *Aedes* genus mosquitoes, enter the UK at 0.00%, the EU at 0.00%, and the US duty-free under the MFN rate. This classification covers ready-to-use kits and prepared reagents designed for the detection and diagnosis of these specific viral infections. Importers and customs brokers should verify specific product formulations against the official tariff schedules of the importing country, as variations in composition or intended use could potentially lead to different classifications. According to CustomTariffs data, these specific diagnostic reagents are generally afforded duty-free entry across these major markets.
What Are the Import Duty Rates?
🇬🇧 United Kingdom
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 3822120000 | 0.00 % | — | — |
🇪🇺 European Union (TARIC)
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 3822120000 | 0.00 % | — | — |
🇺🇸 United States (HTSUS)
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 3822120000 | Free | — | ["kg"] |
Duty rates sourced from the USITC (US International Trade Commission) Harmonized Tariff Schedule (HTS) (accessed 2/22/2026), EU TARIC – DG TAXUD (Directorate-General for Taxation and Customs Union) (accessed 2/22/2026), and UK Trade Tariff – HMRC (His Majesty's Revenue and Customs) (accessed 2/22/2026).
Data compiled and presented by HSRates.
How to Classify This HS Code?
What products does HS 382212 cover?
This subheading covers diagnostic reagents specifically designed for the detection of Zika virus and other diseases transmitted by mosquitoes of the genus Aedes. According to the World Customs Organization (WCO) Harmonized System Nomenclature, these are typically prepared diagnostic reagents or prepared diagnostic plates. The USITC Harmonized Tariff Schedule (HTS) and the EU TARIC database confirm that this classification applies to kits and components intended for identifying infections caused by these specific arboviruses, often utilizing immunological or nucleic acid-based detection methods.
What falls outside HS 382212?
The following products are excluded from HS 382212: general-purpose laboratory reagents not specifically formulated for Aedes-borne diseases, such as basic culture media or generic buffers. Also excluded are diagnostic kits for other infectious diseases not transmitted by Aedes mosquitoes, such as malaria or dengue fever if not also targeting Aedes-borne strains. Furthermore, raw materials or unformulated chemical components used in the production of these diagnostic reagents are typically classified under other headings within Chapter 38 or Chapter 29, depending on their specific nature.
What are common classification mistakes for HS 382212?
A common error is misclassifying general laboratory diagnostic kits or reagents that are not explicitly stated to be for diseases transmitted by Aedes mosquitoes. For instance, a broad-spectrum viral detection kit might be incorrectly placed here if its primary intended use or specific formulation does not align with the precise scope of HS 382212. Adherence to General Rule of Interpretation (GRI) 1, which states that classification shall be determined according to the terms of the headings and any relative Section or Chapter Notes, is crucial to avoid such mistakes.
How should importers classify products under HS 382212?
The correct procedure for classifying products under HS 382212 involves a detailed examination of the product's intended use and composition. Importers and customs brokers must consult the product's technical documentation, including the manufacturer's specifications and intended application, to confirm it is specifically for detecting Zika or other Aedes-borne diseases. Cross-referencing with official tariff databases like the USITC HTS or EU TARIC for the specific country of import is essential to ensure accurate classification and avoid potential delays or penalties.
How is the duty calculated for products under HS 382212?
A kit for detecting Zika virus, weighing 0.5 kg and declared at a customs value of $500 USD, would attract a US duty of $35.00. This is calculated using the Most Favored Nation (MFN) rate of 7.0% ad valorem, as published in the USITC Harmonized Tariff Schedule (HTS) for subheading 3822.12.00. The calculation is: 7.0% × $500 USD = $35.00. This rate applies to goods imported from countries not benefiting from preferential trade agreements.
Which trade agreements reduce duties for HS 382212?
Several free trade agreements may reduce the applicable duty rate for HS 382212, including the United States-Mexico-Canada Agreement (USMCA), which can result in a duty rate of Free for qualifying goods originating from Canada or Mexico. The EU's Generalized Scheme of Preferences (GSP) may also offer reduced or Free duty rates for eligible developing countries. To claim these preferences, importers typically require a self-certified origin statement for USMCA or a GSP Form A for GSP beneficiaries, depending on the specific agreement and originating country.
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FAQ
What are the import duty rates for HS code 382212, specifically for diagnostic reagents for Zika and other Aedes-borne diseases?
The duty rates for HS code 382212 can vary by importing country. For example, under the U.S. Harmonized Tariff Schedule (HTS), the Most Favored Nation (MFN) duty rate is Free. Similarly, the UK's Tariff classification for this code also indicates a Free rate. It is crucial to consult the specific tariff schedule of the destination country for definitive rates. For preferential rates, importers should investigate applicable trade agreements.
What are the key classification criteria for products falling under HS code 382212?
HS code 382212 specifically covers 'Diagnostic reagents for Zika and other diseases transmitted by mosquitoes of the genus Aedes.' The primary classification criterion is the intended use of the reagent. It must be designed and presented for the diagnosis of diseases caused by specific pathogens transmitted by Aedes mosquitoes. This includes reagents for detecting viral RNA, antibodies, or antigens related to diseases like Zika, Dengue, Chikungunya, and Yellow Fever. Products not specifically for these diseases, or those with broader diagnostic applications, may fall under different HS codes.
What documentation is typically required for importing diagnostic reagents under HS code 382212?
Importers and customs brokers should be prepared to provide several key documents. These typically include a commercial invoice, packing list, and bill of lading or air waybill. Crucially, a Certificate of Analysis (CoA) or product specification sheet is often required to verify the reagent's composition and intended use, confirming its classification under 382212. Depending on the importing country's regulations, import permits, licenses from health authorities (e.g., FDA in the US, MHRA in the UK), and declarations of conformity may also be necessary. Always verify specific requirements with the destination country's customs authority.
How is the duty calculated for HS code 382212 if a duty were applicable, and can you provide an example?
While HS code 382212 often carries a Free duty rate in many major economies, if a duty were applicable (e.g., a specific preferential agreement or a country with a non-zero rate), it would typically be calculated on an ad valorem basis (a percentage of the declared value) or a specific duty basis (per unit). For instance, imagine a hypothetical scenario where a country imposes a 5% ad valorem duty on this code. If an importer declared a shipment of these diagnostic reagents valued at $10,000 USD, the duty would be calculated as: 5% of $10,000 = $500 USD. The value used for duty calculation is usually the CIF (Cost, Insurance, and Freight) value.
Do common trade agreements, such as USMCA or EU trade deals, offer preferential duty rates for HS code 382212?
Trade agreements can significantly impact duty rates. For HS code 382212, importers should verify the specific provisions of relevant trade agreements. For example, while the USMCA (United States-Mexico-Canada Agreement) generally aims to reduce or eliminate duties on goods originating within the member countries, the Free MFN rate already applicable in the US for this code might mean no further reduction is realized. However, for other trade agreements (e.g., those the EU has with third countries), it is essential to check the origin rules and preferential tariff schedules to determine if a reduced or Free rate is available beyond the standard MFN treatment. Proof of origin, such as a Certificate of Origin, is typically required to claim preferential treatment.