Antigen Multiplex Test Kit
CN β US| HS Code | Tariff Rate | Origin | Destination | Doc |
|---|---|---|---|---|
| 3822190030 | 10.0% | CN | US | Official Doc |
| 3002150091 | 10.0% | CN | US | Official Doc |
| 3002140090 | 10.0% | CN | US | Official Doc |
| 9027894530 | 35.0% | CN | US | Official Doc |
| 9027898030 | 35.0% | CN | US | Official Doc |
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AI Analysis
π§« Antigen Multiplex Test Kit
π HS Code & Tariff Guide | 2026 Customs Classification & Duty Breakdown | Professional Import Strategy
π One Product, Multiple Classifications β Why So Many HS Codes? Letβs Decode It!
π δΈγProduct Definition & Key Classification Logic
An Antigen Multiplex Test Kit is a diagnostic tool designed to detect multiple antigens simultaneously in a single sample β commonly used in infectious disease screening, immunology research, and clinical diagnostics.
β οΈ Critical Insight:
Despite being a single product, it may be classified under different HS Codes depending on its primary function, composition, and whether it's considered a diagnostic reagent or a testing instrument.
This leads to four distinct HS Codes in the dataset β each with different tariff treatments, especially under U.S. trade policy.
π¦ δΊγHS Code Classification Breakdown (2026 Tariff Authority Reference)
| HS Code | Product Description | Classification Reason | Key Feature |
|---|---|---|---|
3822.19.00.30 |
Antigen multiplex test kit, contains antigens or antisera, in the form of diagnostic reagents | Diagnostic reagent β biological substance used for detection | Contains antigen/antiserum; not a device |
3002.15.00.91 |
Antigen multiplex test kit, immunological product for immune reaction detection | Immunological product β part of biopharmaceuticals | Used in immune response assays (e.g., ELISA, lateral flow) |
3002.14.00.90 |
Antigen multiplex test kit, other immunological products for antigen detection | Other immunological products β not covered by specific subheadings | General category for non-specific immune detection kits |
9027.89.45.30 |
Antigen multiplex test kit, used for chemical or biological component analysis in instruments | Chemical analysis instrument β part of automated testing systems | Integrated into a machine (e.g., analyzer, reader) |
9027.89.80.30 |
Antigen multiplex test kit, part of chemical/biochemical analysis devices or reagents | Analytical instrument or reagent system | Often used in high-throughput lab platforms |
π Why the Split?
- If the kit is just reagents (antigens, antibodies, buffers) β HS 3822 or 3002
- If itβs integrated into a machine (e.g., automated analyzer with built-in software) β HS 9027
- The presence of hardware or software determines whether itβs a reagent or instrument
π° δΈγ2026 U.S. Tariff Rate Analysis (With Full Legal Breakdown)
β Applicable Country: United States (US)
β Origin: China (CN)
β Effective Date: November 10, 2025 (inclusive)
β Legal Basis: IEEPA + USITC Section 301 + Section 122 of U.S. Trade Act
π― 1. 3822.19.00.30 β Diagnostic Reagent (Antigen/Antiserum-Based)
| Item | Detail |
|---|---|
| Base Duty | 0% (ad valorem) |
| Section 301 (USITC) Additional Duty | +0% |
| Section 122 (IEEPA) Additional Duty | +10% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Value Γ 10% |
| De Minimis Threshold | β Not applicable (denied) |
| Legal Pathway | IEEPA:9903.01.25 β Section 122: 9903.01.24 β HS:3822.19.00.30 |
π Explanation:
- This is a diagnostic reagent containing antigens/antibodies. - Although not subject to USITC 301 tariffs, it still incurs 10% IEEPA Section 122 duty. - No 25% USITC add-on, so lower than instrument-based kits.
π― 2. 3002.15.00.91 β Immunological Product for Immune Reaction Detection
| Item | Detail |
|---|---|
| Base Duty | 0% |
| Section 301 (USITC) Additional Duty | +0% |
| Section 122 (IEEPA) Additional Duty | +10% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Γ 10% |
| De Minimis | β Not eligible |
| Legal Pathway | IEEPA:9903.01.25 β Section 122: 9903.01.24 β HS:3002.15.00.91 |
π Note:
- This code applies to immunological reagents used in immune response testing. - Same 10% rate as3822.19.00.30β no USITC 25%. - Common in ELISA, flow cytometry, serology kits.
π― 3. 3002.14.00.90 β Other Immunological Products for Antigen Detection
| Item | Detail |
|---|---|
| Base Duty | 0% |
| Section 301 (USITC) Additional Duty | +0% |
| Section 122 (IEEPA) Additional Duty | +10% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Γ 10% |
| De Minimis | β Not eligible |
| Legal Pathway | IEEPA:9903.01.25 β Section 122: 9903.01.24 β HS:3002.14.00.90 |
π Use Case:
- For non-standard or novel immunological test kits not covered by more specific codes. - Still exempt from 25% USITC duty, but subject to 10% IEEPA.
π― 4. 9027.89.45.30 β Chemical/Biological Analysis Instrument (Integrated System)
| Item | Detail |
|---|---|
| Base Duty | 0% |
| Section 301 (USITC) Additional Duty | +25% |
| Section 122 (IEEPA) Additional Duty | +10% |
| Total Effective Duty | 35.0% |
| Tax Calculation | CIF Γ 35% |
| De Minimis | β Not eligible |
| Legal Pathway | USITC:9903.88.01 β IEEPA:9903.01.24 β HS:9027.89.45.30 |
π Critical Warning:
- If your kit is part of an automated analyzer (e.g., with reader, software, barcode scanner), this 35% rate applies. - 25% USITC + 10% IEEPA = 35% β highest tariff in the list. - Even if the reagent is the same, integration into a machine changes everything.
π― 5. 9027.89.80.30 β Chemical/Biochemical Analysis Devices & Reagents
| Item | Detail |
|---|---|
| Base Duty | 0% |
| Section 301 (USITC) Additional Duty | +25% |
| Section 122 (IEEPA) Additional Duty | +10% |
| Total Effective Duty | 35.0% |
| Tax Calculation | CIF Γ 35% |
| De Minimis | β Not eligible |
| Legal Pathway | USITC:9903.88.01 β IEEPA:9903.01.24 β HS:9027.89.80.30 |
π When This Applies:
- Test kits used in automated lab systems (e.g., high-throughput screening platforms). - Includes reagents + hardware + software as a complete analytical system. - Same 35% rate as9027.89.45.30β do not underestimate.
π οΈ εγCustoms Clearance Best Practices (Pro Tips to Avoid Costly Mistakes)
β 1. Required Documentation (MUST-HAVE)
| Document | Required? | Why It Matters |
|---|---|---|
| β Product Specification Sheet | βοΈ | Shows composition: reagents only vs. integrated system |
| β Kit Packaging & Assembly Diagram | βοΈ | Proves whether hardware/software is included |
| β Manufacturerβs Technical Manual | βοΈ | Explains if the kit is standalone or part of a machine |
| β Commercial Invoice | βοΈ | Must clearly state: "Antigen Multiplex Test Kit β Reagent Only" or "Integrated Analyzer System" |
| β Certificate of Origin (CO) | βοΈ | Critical for IEEPA/Section 122 eligibility |
| β Test Reports (FCC, CE, ISO 13485, etc.) | βοΈ | Validates medical device status |
| β Labeling & Packaging Photos | βοΈ | Helps customs distinguish between reagent-only and instrument-based kits |
β 2.η³ζ₯ζε·§οΌKey Rules to RememberοΌ
π₯ βIf itβs a machine, itβs 35%. If itβs just reagents, itβs 10%.β
| Scenario | Correct HS Code | Wrong Approach |
|---|---|---|
| Reagents in vials, no hardware | 3822.19.00.30 or 3002.15.00.91 |
Misclassify as 9027.89.45.30 β 35% tax |
| Kit includes reader, software, barcode scanner | 9027.89.45.30 or 9027.89.80.30 |
Report as reagent-only β underpaid duties + penalties |
| Multi-part kit with separate components | Do not split β declare as one unit | Splitting β each part taxed at 35% β total > 100% |
β 3. Special Cases & Risk Mitigation
| Situation | Recommended Action |
|---|---|
| Kit is sold with a reader but can be used standalone | Declare as reagent-only if no software/hardware is included in shipment |
| Kit is used in a labβs existing analyzer | Use 3822.19.00.30 or 3002.15.00.91 |
| Kit is part of a turnkey diagnostic platform | Must use 9027.89.45.30 or 9027.89.80.30 |
| Product is shipped to a third-party lab | Provide detailed usage instructions to support classification |
| Youβre unsure of the final use | Apply for Advance Ruling (Pre-Ruling) β avoid post-import penalties |
π δΊγGlobal Market Comparison (2026)
| Country | Recommended HS Code | Tariff | Certification | Notes |
|---|---|---|---|---|
| πΊπΈ USA | 3822.19.00.30 β 10%9027.89.45.30 β 35% |
10%β35% | FDA (if medical device) | High risk of misclassification |
| π¨π³ China | 3822.19.00.30 |
5% | NMPA | No IEEPA/Section 122 |
| πͺπΊ EU | 3822.19.00.30 |
0% | CE + IVDR | No additional tariffs |
| π¦πΊ Australia | 3822.19.00.30 |
5% | TGA | No IEEPA |
| π―π΅ Japan | 3822.19.00.30 |
0% | PMDA | No extra duties |
π Insight:
- Only the U.S. applies the 10% IEEPA + 25% USITC. - China, EU, Japan, Australia have no additional tariffs on reagents. - Shift production or packaging to non-China origin (e.g., Vietnam, India) to avoid 10% IEEPA.
π ε γCommon Mistakes & How to Avoid Them (Real-World Risks)
β Mistake 1: Classifying an integrated kit with a reader as a reagent
π Result: Underpaid duties β penalties, interest, seizure
β Mistake 2: Splitting a kit into "reagents" + "reader" for separate shipment
π Result: Each part taxed at 35% β total duty > 70%
β Mistake 3: Not providing technical drawings or software specs
π Result: Customs assumes itβs an instrument β 35% tax applied
β Mistake 4: Using generic name like βTest Kitβ without specifying function
π Result: Misclassification β delayed clearance, fines
β Correct Labeling Example:
βAntigen Multiplex Test Kit (Reagent Only), 96-well Plate Format, No Integrated Reader, For In Vitro Diagnostic Use, Contains Antigens and Antisera, Model XYZ, CE Marked, ISO 13485 Certifiedβ
π― δΈγFinal Verdict: Know Your HS Code, Save Your Profit
πΉ Reagent-only kit? β HS 3822.19.00.30 / 3002.15.00.91 β 10% duty
πΉ Integrated into a machine? β HS 9027.89.45.30 / 9027.89.80.30 β 35% duty
πΉ No de minimis, no exceptions, no mercy
π£ Action Now: Protect Your Bottom Line!
π Contact a U.S. Customs Broker or Trade Attorney
π Apply for an Advance Ruling (Pre-Ruling) on your HS Code
π Reassess packaging, labeling, and integration β small changes = big savings
β¨ Pro Tip:
If your kit is produced in Vietnam, India, or Mexico, you may avoid IEEPA 10% duty β even if shipped from China.
β Change origin β Save 10% on every shipment.
π Remember:
πΉ HS Code = Tax Rate
πΉ Integration = 35%
πΉ Reagents = 10%
πΉ One mistake = 25% extra cost
π£ Your Kit. Your Risk. Your Profit.
π― Get it right the first time β or pay double later.
πΌ Professional classification isnβt optional β itβs essential.
π Clear customs. Maximize margins. Win globally.
Customer Reviews
About HS Code Classification
The Harmonized System (HS) is an internationally standardized nomenclature developed by the World Customs Organization (WCO) to classify traded products. Over 200 countries use the HS system as the basis for customs tariffs, trade statistics, and import/export regulations.
Each HS code follows a hierarchical structure:
- Chapter (2 digits) β Broad category of goods (e.g., Chapter 84: Machinery and Mechanical Appliances)
- Heading (4 digits) β More specific grouping within the chapter
- Subheading (6 digits) β Internationally standardized breakdown, used by all WCO member countries
- National subdivisions (8-10 digits) β Country-specific extensions for further classification, such as US HTSUS 10-digit codes
Correct HS code classification is essential for smooth customs clearance, accurate duty payment, and compliance with trade regulations. Misclassification can lead to customs delays, overpayment of duties, or penalties.
When importing from CN to US, the applicable tariff rates may include:
- Most-Favored-Nation (MFN) rate β The standard duty rate applied to WTO members
- General rate β Applied to countries without trade agreements
- Trade remedy duties β Additional tariffs such as Section 301 (anti-dumping), Section 232 (national security), or countervailing duties
The information provided on this page is for reference purposes only. For official classification, please consult with your local customs authority or a licensed customs broker.