HS 382213 For blood-grouping
Quick Answer: Diagnostic reagents for blood-grouping imported under HS 382213 enter the UK at 0.00%, the EU at 0.00%, and the US duty-free under the MFN rate. This Harmonized System code specifically covers prepared diagnostic reagents designed for determining blood groups, typically used in medical laboratories and blood banks. These reagents are crucial for safe blood transfusions and compatibility testing. Importers should verify specific product formulations against the WCO Explanatory Notes and relevant national customs regulations to ensure correct classification. According to CustomTariffs data, these products generally benefit from preferential duty treatment across major trading blocs, simplifying import processes.
What Are the Import Duty Rates?
🇬🇧 United Kingdom
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 3822130000 | 0.00 % | — | — |
🇪🇺 European Union (TARIC)
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 3822130000 | 0.00 % | — | — |
🇺🇸 United States (HTSUS)
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 3822130000 | 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 Has Trade Volume Developed?
Trade Volume 2023
How to Classify This HS Code?
What products does HS 382213 cover?
This subheading covers diagnostic reagents specifically designed for blood-grouping. According to the World Customs Organization's Harmonized System Nomenclature, these are preparations used to determine the blood group of an individual, often involving antibodies or antigens that react with specific blood components. The US International Trade Commission (USITC) Harmonized Tariff Schedule (HTS) and the EU's TARIC database confirm that these reagents are typically presented in a form ready for use in laboratory or clinical settings for serological testing to identify ABO and Rh blood types, crucial for transfusions and compatibility testing.
What falls outside HS 382213?
The following products are excluded from HS 382213: general laboratory reagents not specifically for blood-grouping, such as basic chemical solutions or stains used in microscopy; diagnostic kits for other medical conditions like pregnancy tests or infectious disease detection; and blood collection or processing materials. For instance, sterile vacuum tubes for blood collection (HS 9018.90) or general purpose laboratory chemicals (Chapter 28 or 29) would be classified elsewhere, as they do not meet the specific diagnostic purpose of blood-grouping reagents.
What are common classification mistakes for HS 382213?
A common error is misclassifying general diagnostic reagents or kits that include blood-grouping components but are primarily intended for broader diagnostic purposes. For example, a comprehensive medical diagnostic kit that contains blood-grouping reagents alongside other tests might be incorrectly classified under 382213 if its primary function is not solely blood-grouping. Following General Rule of Interpretation (GRI) 3(b) for mixtures or composite goods, the classification should reflect the essential character of the product, which for 382213 must be its specific blood-grouping function.
How should importers classify products under HS 382213?
The correct procedure for classifying products under HS 382213 involves a thorough examination of the product's intended use and composition. Importers and customs brokers must verify that the reagent is explicitly formulated and marketed for blood-grouping. Reviewing the product's technical documentation, including its Safety Data Sheet (SDS) and manufacturer's specifications, is essential. Consulting the official tariff schedules of the importing country, such as the USITC HTS or the UK Trade Tariff, and cross-referencing with WCO Explanatory Notes will ensure accurate classification.
How is the duty calculated for products under HS 382213?
A shipment of 100 vials of Anti-A blood grouping reagent, 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) duty rate of 7.0% ad valorem, as published in the USITC Harmonized Tariff Schedule for HTS code 3822.13.0000. The calculation is: 7.0% of $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 382213?
Several free trade agreements may reduce the applicable duty rate for HS 382213, including the United States-Mexico-Canada Agreement (USMCA), which can result in a Free duty rate for eligible goods originating from Canada and Mexico. The EU's Generalised Scheme of Preferences (GSP) also offers reduced or Free duty rates for eligible products from developing countries. To claim these preferences, importers typically require a self-certified origin statement for USMCA or a EUR.1 movement certificate for certain EU preferences, depending on the specific agreement and originating country.
```Which HS Codes Are Related?
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FAQ
What are the typical import duty rates for HS code 382213, 'Diagnostic reagents for blood-grouping'?
For HS code 382213, the Most Favored Nation (MFN) duty rate in the United States is 0.00%. In the European Union, under the TARIC system, the rate is also 0.00%. The United Kingdom's Trade Tariff also lists this classification as Free. These rates are generally applied as ad valorem (percentage of value) or specific duties, but for this code, the duties are typically zero.
What specific criteria must diagnostic reagents meet to be classified under HS code 382213?
To be classified under HS code 382213, the diagnostic reagents must be specifically intended for the determination of blood groups. This includes reagents used for identifying ABO, Rh, and other blood group antigens. The key is their direct application in serological testing for blood typing purposes. Products not specifically designed for blood-grouping, even if related to blood analysis, may fall under different HS codes.
What documentation is typically required for importing diagnostic reagents for blood-grouping (HS 382213)?
Importers and customs brokers should be prepared to provide a commercial invoice, packing list, and bill of lading or air waybill. Additionally, a Certificate of Analysis (CoA) from the manufacturer is often required to verify the product's composition and intended use, confirming it meets the criteria for HS 382213. Depending on the importing country's regulations, specific import licenses or permits from health authorities (e.g., FDA in the US, EMA in the EU) may also be necessary for medical diagnostic reagents.
How is the duty calculated for HS code 382213, and can you provide an example?
Since the duty rates for HS code 382213 are typically 0.00% (Free) in major markets like the US, EU, and UK, the calculation results in zero duty. For instance, if a shipment of diagnostic reagents for blood-grouping valued at $10,000 is imported into the United States, the MFN duty would be calculated as: $10,000 (Value) × 0.00% (Duty Rate) = $0.00 (Duty). Even if a specific duty were applicable (e.g., per unit), the rate would need to be applied to the relevant quantity.
Do trade agreements, such as USMCA or EU trade deals, offer preferential duty rates for HS code 382213?
Given that the standard duty rates for HS code 382213 are already 0.00% (Free) under the MFN tariff in many countries, preferential rates under trade agreements like the USMCA (United States-Mexico-Canada Agreement) or various EU Free Trade Agreements (FTAs) are unlikely to provide further reductions. However, importers should always verify the specific terms of any applicable trade agreement and ensure they meet all rules of origin requirements to claim any potential benefits, even if the current duty is zero, as this can streamline customs clearance.