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Reagent Kit

CN β†’ US
HS Code Tariff Rate Origin Destination Doc
3006931000 10.0% CN US Official Doc
3006938000 40.0% CN US Official Doc
3002150091 10.0% CN US Official Doc
3002140090 10.0% CN US Official Doc
3822190080 10.0% CN US Official Doc

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πŸ§ͺ Reagent Kit (试剂盒)


🌐 HS Code Reference & Customs Clearance Guide | 2026 Latest Tariff Analysis | Professional Clearance Strategy
πŸ“Œ I. Product Definition & Classification: Do You Really Understand "Reagent Kits"?

A Reagent Kit is a collection of reagents, controls, and/or calibrators packaged together for use in diagnostic, clinical, or laboratory settings. In international trade, its classification depends heavily on its intended use (e.g., clinical trials, diagnostic testing) and composition (biological vs. chemical).

⚠️ Key Distinction:
- If it is part of a clinical trial kit (placebo/blinding), it may fall under 3006.93.
- If it is an immunological/biological product, it may fall under 3002.1x.
- If it is a general diagnostic/chemical reagent, it may fall under 3822.19.


πŸ“¦ II. HS Code Classification Details (2026 Latest Tariff Authority Comparison)

HS Code Product Description Applicable Scenario Material/Composition
3006.93.10.00 Clinical Trial Kits Kits used as placebos or blinding agents in clinical trials, packaged with drug formulations Medical supplies, non-material conflict
3006.93.80.00 Other Clinical Trial Kits Kits containing "other chemical substances" besides drugs; assumed chemical-based due to lack of material specification Chemical preparations
3002.15.00.91 Other Immunological Products Reagent kits inferred as immunological or biochemical products; matches "other immunological products" Biological/Immunological
3002.14.00.90 Other Immunological Products Kits inferred as immunological nature; categorized under "Other" with no obvious material conflict Biological/Immunological
3822.19.00.80 Diagnostic/Laboratory Reagents Reagent kits for diagnostic or laboratory testing; fits the scope of diagnostic reagents Chemical/Laboratory

πŸ” Key Reminder:
- 3006.93 is for Clinical Trial Kits (Placebo/Blinding).
- 3002.1x is for Immunological/Biological Reagents.
- 3822.19 is for General Diagnostic/Laboratory Chemical Reagents.
- Classification depends on specific product attributes not fully detailed in the name "Reagent Kit."


πŸ’° III. 2026 Latest Tariff Rate Details (Including Surcharges, Policy Add-ons)

βœ… Applicable Country: United States (US)
βœ… Origin: China (CN)
βœ… Effective Time: From November 10, 2025 (including subsequent imports)

🎯 1. 3006.93.10.00 β€”β€” Clinical Trial Kits (Placebo/Blinding)

Item Content
Base Tariff 0.0% (ad valorem)
USITC Additional Tariff +0.0%
Section 122 Tariff +10% (Targeting China/Hong Kong products)
Total Tariff 10.0%
Tax Calculation CIF Value Γ— 10.0%
De Minimis Eligibility ❌ Not Applicable (Standard clinical trial kits usually exceed de minimis value or are restricted)
Legal Basis Path Section 122: 10% β†’ USITC: 3006.93.10.00

πŸ“Œ Explanation:
- Base Tariff 0%: Clinical trial kits often enjoy zero base duty.
- Section 122 Tariff 10%: This is a specific additional tariff applied to certain imports from China/Hong Kong.
- Total 10%: Relatively low compared to other categories, but still significant for high-value trials.


🎯 2. 3006.93.80.00 β€”β€” Other Clinical Trial Kits (Chemical-Based)

Item Content
Base Tariff 5.0%
USITC Additional Tariff +25.0% (From USITC Footnote 9903.88.01 / Section 301)
Section 122 Tariff +10% (Targeting China/Hong Kong products)
Total Tariff 40.0%
Tax Calculation CIF Value Γ— 40.0%
De Minimis Eligibility ❌ Not Applicable
Legal Basis Path IEEPA: 25% β†’ Section 122: 10% β†’ USITC: 3006.93.80.00

πŸ“Œ Explanation:
- Base Tariff 5%: Higher base duty for "other" chemical-based kits.
- USITC 25%: Section 301 tariff on Chinese goods.
- Section 122 10%: Additional tariff.
- Total 40%: Extremely high tariff. Must be carefully evaluated for cost efficiency.


🎯 3. 3002.15.00.91 β€”β€” Other Immunological Products

Item Content
Base Tariff 0.0%
USITC Additional Tariff +0.0%
Section 122 Tariff +10%
Total Tariff 10.0%
Tax Calculation CIF Value Γ— 10.0%
De Minimis Eligibility ❌ Not Applicable
Legal Basis Path Section 122: 10% β†’ USITC: 3002.15.00.91

πŸ“Œ Explanation:
- Base Tariff 0%: Immunological products often have zero base duty.
- Section 122 10%: The only additional cost.
- Total 10%: Competitive rate for biological/immunological reagents.


🎯 4. 3002.14.00.90 β€”β€” Other Immunological Products

Item Content
Base Tariff 0.0%
USITC Additional Tariff +0.0%
Section 122 Tariff +10%
Total Tariff 10.0%
Tax Calculation CIF Value Γ— 10.0%
De Minimis Eligibility ❌ Not Applicable
Legal Basis Path Section 122: 10% β†’ USITC: 3002.14.00.90

πŸ“Œ Explanation:
- Similar to 3002.15.00.91, this category also enjoys 0% base tariff.
- Total 10%: Driven solely by the Section 122 tariff.


🎯 5. 3822.19.00.80 β€”β€” Diagnostic/Laboratory Reagents

Item Content
Base Tariff 0.0%
USITC Additional Tariff +0.0%
Section 122 Tariff +10%
Total Tariff 10.0%
Tax Calculation CIF Value Γ— 10.0%
De Minimis Eligibility ❌ Not Applicable
Legal Basis Path Section 122: 10% β†’ USITC: 3822.19.00.80

πŸ“Œ Explanation:
- Base Tariff 0%: General diagnostic reagents often have zero base duty.
- Section 122 10%: The only additional cost.
- Total 10%: Most cost-effective for general chemical-based diagnostic kits.


πŸ› οΈ IV. Customs Clearance Practical Advice (Battle-Tested Pitfall Guide)

βœ… 1. Documentation Checklist (None of the Above is Optional)

Document Required Description
βœ… Product Specification Sheet βœ”οΈ Must detail composition (chemical vs. biological), intended use (diagnostic vs. clinical trial), and format.
βœ… Composition Declaration βœ”οΈ Explicitly state if the kit contains immunological substances, chemicals, or placebos.
βœ… Product Photos βœ”οΈ Clear images of packaging, labels, and contents (vials, cards, etc.).
βœ… Third-Party Test Reports βœ”οΈ FDA 510(k), CE Mark, or ISO 13485 certificates (if applicable for medical devices).
βœ… Commercial Invoice βœ”οΈ Must clearly state "Reagent Kit for [Diagnostic/Clinical Trial] Use" and HS Code.
βœ… Certificate of Origin (CO) βœ”οΈ Critical for proving origin to apply/avoid Section 122 tariffs.
βœ… Packing List βœ”οΈ Detail contents to avoid misclassification claims.

βœ… 2. Declaration Tips (Key Mantra)

πŸ”₯ "Know Your Use, Declare Your Nature, Avoid 40%!"

Scenario Correct Declaration Wrong Practice
Clinical Trial Kit (Placebo) 3006.93.10.00 Misdeclare as general reagent β†’ Risk of audit
Clinical Trial Kit (Chemical) 3006.93.80.00 Fail to declare chemical nature β†’ 40% tariff + penalty
Immunological/Biological Kit 3002.15.00.91 or 3002.14.00.90 Declare as chemical reagent β†’ Misclassification risk
General Diagnostic Kit 3822.19.00.80 Declare as medical device β†’ Delays

βœ… 3. Special Case Handling

Situation Handling Advice
Mixed Contents (Drug + Reagent) If packaged together for clinical trials, consider 3006.93. If separate, declare separately.
Biological vs. Chemical Immunological β†’ 3002.1x (10%). Chemical β†’ 3822.19 (10%) or 3006.93.80 (40%). Proof of composition is key!
High-Value Kits Due to 40% tariff on 3006.93.80, consider if 3822.19 or 3002.1x is more appropriate based on actual content.
New Product Category Apply for Advance Ruling to confirm HS Code and tariff rate before shipment.

🌍 V. Global Major Market Clearance Comparison (2026 Latest)

Country/Region Recommended HS Code Tariff (China Origin) Certification Requirements Notes
πŸ‡ΊπŸ‡Έ United States 3006.93.10.00 / 3822.19.00.80 10% (Most cases) / 40% (Some clinical) FDA 510(k), CE (if EU-origin) Section 122 + 301 tariffs apply. High risk for chemical clinical kits.
πŸ‡¨πŸ‡³ China 3006.93 / 3822.19 5% - 10% NMPA Approval No additional US-style surcharges.
πŸ‡ͺπŸ‡Ί European Union 3822.00 / 3006.93 0% - 2% CE Mark, ISO 13485 No Section 122 or 301 tariffs. Most cost-effective for reagents.
πŸ‡¦πŸ‡Ί Australia 3822.19 5% TGA Approval No additional surcharges.
πŸ‡―πŸ‡΅ Japan 3822.19 0% - 5% PMDA Approval No additional surcharges.

πŸ“Œ Conclusion:
- The US is the only market with high additional tariffs (up to 40%) for certain reagent kits.
- EU, Japan, and Australia offer significantly lower tariff burdens (0-5%).
- Cost-saving Strategy: If possible, route shipments through non-China origins or ensure classification under 10% tariff categories (3006.93.10, 3002.x, 3822.19). Avoid 3006.93.80 if alternative classification is viable.


πŸ“Œ VI. Common Mistakes & Pitfall Guide (Lessons Learned)

❌ Mistake 1: Classifying a Chemical-Based Clinical Kit as 3822.19 (10%) instead of 3006.93.80 (40%)
πŸ‘‰ Consequence: Audit, back taxes, and penalties if content proves it's a clinical kit with chemical reagents.

❌ Mistake 2: Assuming all Reagent Kits are 3822.19 (10%)
πŸ‘‰ Consequence: If the kit is immunological, it should be 3002.1x (10%). If it's a clinical trial kit, it might be 3006.93. Misclassification leads to delays.

❌ Mistake 3: Omitting Composition Details on Invoice
πŸ‘‰ Consequence: Customs cannot determine if it's chemical, biological, or placebo β†’ 100% inspection, delays, and potential misclassification.

βœ… Correct Practice:

"Reagent Kit for Diagnostic Use, Chemical Basis, Model XYZ, CE Marked" β†’ 3822.19.00.80
"Reagent Kit for Clinical Trial, Placebo Component, Model ABC" β†’ 3006.93.10.00
"Immunological Assay Kit, Enzyme-Linked, Model DEF" β†’ 3002.15.00.91


🎯 VII. Conclusion: Precise Classification, Cost Optimization!

🎯 Remember the Mantra:

πŸ”Ή "Clinical Trial? Check 3006.93. Biological? 3002.1x. Chemical Diagnostic? 3822.19. Avoid 3006.93.80 at all costs!"
πŸ”Ή "10% vs. 40% is a huge difference. Document your composition clearly!"


πŸ“Œ Pro Tip:
If your reagent kits are originating from Vietnam, Mexico, or Thailand, you may be eligible for IEEPA/Section 301 exemptions or lower tariffs.
Recommendation: Apply for an Advance Ruling from US Customs (CBP) to confirm the correct HS Code and tariff rate before shipment.


πŸ“£ Immediate Action:

πŸ“ž Contact Professional Customs Broker + Provide Product Specs + Apply for HS Code Advance Ruling
πŸš€ Ensure your Reagent Kits clear customs smoothly, minimize costs, and maximize profit!


✨ Professional Clearance Starts with Accurate Classification!
πŸ’Ό Every Cent of Your Cost Deserves Precise Calculation!

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.