ELISA Reagent Card
CN β US| HS Code | Tariff Rate | Origin | Destination | Doc |
|---|---|---|---|---|
| 3006305000 | 10.0% | CN | US | Official Doc |
| 3822190030 | 10.0% | CN | US | Official Doc |
| 3006301000 | 10.0% | CN | US | Official Doc |
| 3822190080 | 10.0% | CN | US | Official Doc |
Product Images
AI Analysis
π§ͺ ELISA Reagent Card β HS Code & Tariff Guide 2026 | Full Customs Clearance Strategy
π HS Code Reference & Customs Clearance Master Guide | 2026 Updated Tariff Rules | Pro-Level Import Strategy
π I. Product Definition & Classification: What Exactly Is an ELISA Reagent Card?
An ELISA Reagent Card is a diagnostic test device used in clinical laboratories and medical research to detect the presence of specific antigens or antibodies in biological samples (e.g., blood, serum, urine). It typically contains:
- Pre-coated antigens or antibodies on a solid-phase membrane or strip
- Enzyme-labeled detection reagents
- Colorimetric substrate for signal development
- Sample wells and control zones
β οΈ Key Classification Insight:
- If the card is intended for diagnostic use in humans, it falls under diagnostic reagents
- If it contains antigen/antibody components and is used for laboratory testing, it qualifies as a diagnostic or laboratory reagent
- It is not a general chemical β itβs a purpose-built diagnostic tool
π¦ II. HS Code Classification Breakdown (2026 Official Tariff Schedule)
| HS Code | Product Description | Applicable Use Case | Matches Diagnostic Purpose? |
|---|---|---|---|
3006.30.50.00 |
Diagnostic reagents, including those used in immunoassays like ELISA, intended for human use | Clinical diagnostics, hospital labs, medical testing | β Yes β Direct match |
3822.19.00.30 |
Other chemical products, not elsewhere specified, including diagnostic or lab reagents with antigen/antibody components | Research use, non-clinical testing, R&D kits | β Yes β Broad category fit |
3006.30.10.00 |
Diagnostic reagents, specifically for in vitro use, including immunological reagents | Medical testing, disease screening, pregnancy tests | β Yes β No material/shape conflict |
3822.19.00.80 |
Other chemical products, used as carriers or supports for diagnostic or laboratory reagents | Reagent card substrates, membranes, or backing materials | β Yes β Functional role in test delivery |
π Critical Note:
- All four HS Codes are valid for ELISA Reagent Cards depending on intended use, content, and form
- The best fit depends on documentation and labeling β not just the physical card
π° III. 2026 Tariff Rate Analysis (With Full Legal & Policy Breakdown)
β Applicable Country: United States (US)
β Origin: China (CN)
β Effective Date: November 10, 2025 (including subsequent imports)
π― 1. 3006.30.50.00 β Diagnostic Reagents (Human Use)
| Item | Detail |
|---|---|
| Base Duty | 0.0% (ad valorem) |
| Additional Tariff (Section 301) | 0.0% |
| Section 122 Tariff (IEEPA) | 10.0% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Value Γ 10.0% |
| De Minimis Threshold | β Not applicable (denied) |
| Legal Basis Path | IEEPA: 9903.01.25 β Section 122: 10% β HS: 3006.30.50.00 |
π Explanation:
- This code is specifically for diagnostic reagents used in human testing
- The 10% tariff comes from Section 122 of the Trade Act of 1974, which authorizes the President to impose tariffs on imports from countries engaging in unfair trade practices
- No additional 301 or Section 321 tariffs apply here β only the 10% IEEPA-based Section 122 tariff
π― 2. 3822.19.00.30 β Other Chemicals (Diagnostic/Lab Reagents)
| Item | Detail |
|---|---|
| Base Duty | 0.0% |
| Additional Tariff (Section 301) | 0.0% |
| Section 122 Tariff (IEEPA) | 10.0% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Γ 10.0% |
| De Minimis Threshold | β Not applicable |
| Legal Basis Path | IEEPA: 9903.01.25 β Section 122: 10% β HS: 3822.19.00.30 |
π Explanation:
- This code applies when the reagent card is not explicitly classified as a diagnostic reagent, but still contains antigen/antibody components
- Commonly used when labeling is ambiguous or no medical claims are made
- Still subject to 10% Section 122 tariff due to China origin
π― 3. 3006.30.10.00 β Diagnostic Reagents (In Vitro Use)
| Item | Detail |
|---|---|
| Base Duty | 0.0% |
| Additional Tariff (Section 301) | 0.0% |
| Section 122 Tariff (IEEPA) | 10.0% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Γ 10.0% |
| De Minimis Threshold | β Not applicable |
| Legal Basis Path | IEEPA: 9903.01.25 β Section 122: 10% β HS: 3006.30.10.00 |
π Explanation:
- This is the most precise code for ELISA cards used in in vitro diagnostics (IVD)
- No material or form conflict β cards are standard for IVD testing
- The 10% tariff is identical to the others β no difference in rate, but better classification accuracy
π― 4. 3822.19.00.80 β Other Chemicals (Carrier/Support for Reagents)
| Item | Detail |
|---|---|
| Base Duty | 0.0% |
| Additional Tariff (Section 301) | 0.0% |
| Section 122 Tariff (IEEPA) | 10.0% |
| Total Effective Duty | 10.0% |
| Tax Calculation | CIF Γ 10.0% |
| De Minimis Threshold | β Not applicable |
| Legal Basis Path | IEEPA: 9903.01.25 β Section 122: 10% β HS: 3822.19.00.80 |
π Explanation:
- Used when the card is seen as a substrate or carrier (e.g., nitrocellulose membrane) rather than a diagnostic reagent
- Applies if no antigen/antibody is pre-coated or if the card is sold as a blank support
- Still triggers 10% Section 122 tariff due to origin
π οΈ IV. Customs Clearance Best Practices (Pro Tips to Avoid Delays & Penalties)
β 1. Essential Documentation (Must-Have Checklist)
| Document | Required? | Purpose |
|---|---|---|
| β Product Technical Specification | βοΈ | Prove antigen/antibody content, intended use |
| β Labeling & Packaging Photos | βοΈ | Show "For In Vitro Diagnostic Use" or "ELISA Reagent" |
| β Manufacturerβs Certificate | βοΈ | Confirm origin, composition, and intended use |
| β Commercial Invoice | βοΈ | Clearly state: βELISA Reagent Card, For In Vitro Diagnostic Useβ |
| β Certificate of Origin (CO) | βοΈ | Required for tariff determination |
| β FDA 510(k) or CE Mark (if applicable) | βοΈ | For medical-grade reagents |
| β Lab Test Reports (e.g., sensitivity, specificity) | βοΈ | Support diagnostic claim |
β 2.η³ζ₯ζε·§οΌη³ζ₯ε£θ―οΌ
π₯ βDiagnostic claim? Use 3006.30.10.00 or 3006.30.50.00 β no guesswork!β
| Scenario | Correct HS Code | Wrong Code | Risk |
|---|---|---|---|
| Card has antibodies pre-coated, labeled for medical testing | 3006.30.10.00 or 3006.30.50.00 |
3822.19.00.30 |
Higher audit risk |
| Card is blank membrane, used as support | 3822.19.00.80 |
3006.30.10.00 |
Misclassification |
| No medical claims, only for research | 3822.19.00.30 |
3006.30.50.00 |
Overpayment risk |
| Selling as kit with reagents + card | Bundle as one unit | Split into parts | Tax up to 89.5% |
β 3. Special Cases & Handling
| Situation | Recommended Action |
|---|---|
| Reagent card with embedded software or reader | Still classify as reagent β use 3006.30.10.00 |
| Used in veterinary or agricultural testing | Use 3822.19.00.30 or 3822.19.00.80 |
| Exported to EU, UK, or Australia | Use 3006.30.10.00 β 0% tariff (no Section 122) |
| Imported from Vietnam, Mexico, or India | May qualify for IEEPA exemption β 0% tariff |
| Requesting a Pre-Ruling (Advance Ruling) | β Highly recommended β avoid future disputes |
π V. Global Customs Comparison (2026 Update)
| Country | Recommended HS Code | Tariff | Certification | Notes |
|---|---|---|---|---|
| πΊπΈ USA | 3006.30.10.00 or 3006.30.50.00 |
10.0% (Section 122) | FDA, CE (if applicable) | No de minimis |
| π¨π³ China | 3006.30.10.00 |
5% | CCC, ISO 13485 | No extra tariffs |
| πͺπΊ EU | 3006.30.10.00 |
0% (if CE marked) | CE, ISO 13485 | No Section 122 |
| π¦πΊ Australia | 3006.30.10.00 |
0% | RCM | No extra tariffs |
| π―π΅ Japan | 3006.30.10.00 |
0% | PSE, JIS | No additional duties |
π Key Insight:
- Only the US applies the 10% Section 122 tariff to ELISA reagent cards from China
- All other major markets treat them as standard medical reagents with 0% or low tariffs
π VI. Common Mistakes & How to Avoid Them (Real-World Pitfalls)
β Mistake 1: Labeling card as βChemical Reagentβ instead of βDiagnostic Reagentβ
π Result: Misclassified as 3822.19.00.30 β higher audit risk
β
Fix: Use βFor In Vitro Diagnostic Useβ on packaging and invoice
β Mistake 2: Splitting card + reagents into separate shipments
π Result: Each item taxed at up to 89.5% β Total tax over 200%
β
Fix: Ship as one kit under a single HS Code
β Mistake 3: Not providing technical specs or test reports
π Result: Customs may delay or reject the entry
β
Fix: Attach sensitivity/specificity data and manufacturerβs letter
β Mistake 4: Using βELISA Stripβ or βTest Cardβ without context
π Result: Unclear intent β misclassification risk
β
Fix: Use full phrase: βELISA Reagent Card, For In Vitro Diagnostic Use, Containing Pre-Coated Antibodiesβ
π― VII. Final Verdict: How to Win the Clearance Game
πΉ Best HS Code:
3006.30.10.00or3006.30.50.00β most accurate, lowest risk
πΉ Worst Case:3822.19.00.80β only if card is purely a carrier
πΉ Total Tariff: Always 10.0% in the US (due to Section 122) β no variation
πΉ De Minimis? β Not available β must pay full 10%
π£ Take Action Now: Avoid Costly Mistakes!
π Contact a licensed customs broker + request an HS Code pre-ruling
π Use a professional tariff calculator with real-time IEEPA/Section 122 rules
π Prepare full documentation β donβt wait until customs asks
β¨ Pro Tip:
If your ELISA Reagent Cards are originating from Vietnam, Mexico, or India, you may qualify for IEEPA exemption β 0% tariff in the US.
π Apply for a Certificate of Origin and file a tariff exclusion request if needed.
π― Conclusion: Precision Matters. One Wrong Code = Thousands in Extra Cost!
πΉ βDiagnostic? Use 3006.30.10.00 β not 3822.19.00.30!β
πΉ β10% tariff? Yes β but only in the US, and only for China-origin goods.β
πΉ βNever split a kit β one HS Code, one invoice, one happy customs officer.β
πΌ Your productβs success starts with the right HS Code.
π¦ Your profits depend on accurate classification.
π Get it right β and ship with confidence!
β Professional Clearance. Zero Surprises. Maximum Efficiency.
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.