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antigen rapid test kit

CN → US
HS编码 关税税率 原产国 目的国 文档
3822190030 10.0% CN US 官方文档
3002150091 10.0% CN US 官方文档
3002140090 10.0% CN US 官方文档
9027894530 35.0% CN US 官方文档
9027898030 35.0% CN US 官方文档

商品图片

AI分析

🧫 Antigen Rapid Test Kit (ARTK)


🌐 HS Code & Tariff Guide | 2026 U.S. Trade Compliance | Full Duty Breakdown & Customs Strategy
📌 One Product, Five HS Codes — Know the Difference to Avoid 45%+ Tariff Traps!


📌 1. Product Definition & Classification: What Is an Antigen Rapid Test Kit?

An Antigen Rapid Test Kit (ARTK) is a point-of-care diagnostic device used to detect specific viral antigens (e.g., SARS-CoV-2, influenza) in human samples (nasal swabs, saliva) within minutes. It typically includes:

  • A test strip with immobilized antibodies
  • A sample buffer
  • A cassette or card housing the reaction zone
  • A pipette or dropper for sample application

⚠️ Key Distinction:
- If the product contains antigen-specific reagents (antibodies, conjugates, buffers) → It's a diagnostic/immunological reagent
- If it's a standalone instrument with built-in detection (e.g., optical reader) → It's a chemical analyzer


📦 2. HS Code Classification Breakdown (2026 U.S. Tariff Schedule)

HS Code Product Description Classification Logic Tax Rate Duty Type
3822.19.00.30 Reagents for antigen detection, containing antigens or antibody-antigen complexes Contains antigen-specific reagents; used in diagnostic testing; no conflict with materials 10.0% 122条款关税
3002.15.00.91 Immunological products, including antigen detection kits Core function: immunological reaction; fits “other immunological products” 10.0% 122条款关税
3002.14.00.90 Immune reaction reagents, used in immunodiagnostics Matches “other immunological products” category; diagnostic use 10.0% 122条款关税
9027.89.45.30 Chemical or biochemical analysis instruments, used for antigen detection Instrument-based detection system (e.g., lateral flow reader) 35.0% 25% + 10%
9027.89.80.30 Chemical analysis apparatus, applied in immunological assays Used for immunochemical analysis; fits chemical analysis logic 35.0% 25% + 10%

🔍 Critical Insight:
- Reagents-only kits (test strips + buffer) → 3822.19.00.30 / 3002.15.00.91 / 3002.14.00.9010% total
- Instrument + test kit combo (e.g., reader + cassette) → 9027.89.45.30 / 9027.89.80.3035% total
- Do NOT mix reagents and instruments in one申报 — risk of misclassification and 35% duty on reagents!


💰 3. 2026 U.S. Tariff Breakdown (Detailed & Compliant)

Applicable Country: China (CN)
Effective Date: November 10, 2025 (per U.S. Trade Act 2025)
Legal Basis: IEEPA + USITC Section 301 + 122条款 (Section 122 of U.S. Trade Act)


🎯 1. 3822.19.00.30 — Reagents for Antigen Detection

Item Detail
Base Tariff 0.0% (ad valorem)
USITC 301 Tariff 0.0%
122条款 Tariff 10.0%
Total Duty 10.0%
Duty Calculation CIF × 10.0%
De Minimis Exemption Not eligible (denied under 122条款)
Legal Pathway IEEPA:9903.01.25122条款:3822.19.00.30FOOTNOTE:9903.88.01

📌 Why 10%?
- The product is not a medical device, but a diagnostic reagent.
- Classified under 3822.19.00.30 as a “reagent containing antigens” — not a finished medical device.
- 122条款 applies to non-medical diagnostic reagents from China — 10% flat rate.


🎯 2. 3002.15.00.91 — Immunological Products (Antigen Detection Kits)

Item Detail
Base Tariff 0.0%
USITC 301 Tariff 0.0%
122条款 Tariff 10.0%
Total Duty 10.0%
Duty Calculation CIF × 10.0%
De Minimis ❌ Not eligible
Legal Pathway IEEPA:9901.25122条款:3002.15.00.91FOOTNOTE:9903.88.01

📌 Why 10%?
- The kit performs immunological reactions (antibody-antigen binding).
- Falls under “other immunological products” (3002.15.00.91).
- 122条款 applies — 10% on all such reagents from China.


🎯 3. 3002.14.00.90 — Immune Reaction Reagents (Diagnostic Use)

Item Detail
Base Tariff 0.0%
USITC 301 Tariff 0.0%
122条款 Tariff 10.0%
Total Duty 10.0%
Duty Calculation CIF × 10.0%
De Minimis ❌ Not eligible
Legal Pathway IEEPA:9903.01.24122条款:3002.14.00.90FOOTNOTE:9903.88.01

📌 Why 10%?
- The product is a reagent used in immune reactionsnot a device.
- Matches “other immunological products” under 3002.14.00.90.
- 122条款 applies — 10%.


🎯 4. 9027.89.45.30 — Chemical/Biochemical Analysis Instruments (e.g., Lateral Flow Reader)

Item Detail
Base Tariff 0.0%
USITC 301 Tariff 25.0%
122条款 Tariff 10.0%
Total Duty 35.0%
Duty Calculation CIF × 35.0%
De Minimis ❌ Not eligible
Legal Pathway IEEPA:9903.01.25USITC:9027.89.45.30122条款:9027.89.45.30

📌 Why 35%?
- USITC 301 Tariff (25%): Applies to all chemical/biochemical analysis instruments from China.
- 122条款 (10%): Applies to all such instruments under Section 122.
- Total: 35%Extremely highavoid this classification unless the product is truly an instrument.


🎯 5. 9027.89.80.30 — Chemical Analysis Apparatus (Immunological Use)

Item Detail
Base Tariff 0.0%
USITC 301 Tariff 25.0%
122条款 Tariff 10.0%
Total Duty 35.0%
Duty Calculation CIF × 35.0%
De Minimis ❌ Not eligible
Legal Pathway IEEPA:9903.01.24USITC:9027.89.80.30122条款:9027.89.80.30

📌 Why 35%?
- The product is used in immunochemical analysis — fits “chemical analysis apparatus”.
- USITC 25% + 122条款 10% = 35%
- Do NOT apply this to a test kit alone — only if it’s a standalone instrument.


🛠️ 4. Customs Clearance Best Practices (Pro Tips)

✅ 1. Documentation Checklist (MUST-HAVE)

Document Required? Purpose
✅ Product Specification Sheet ✔️ Show reagent composition, antigen type, detection method
✅ Test Strip Diagram / Flow Chart ✔️ Prove it’s a reagent, not an instrument
✅ Product Photos (Clear Labeling) ✔️ Show “Test Kit”, “Reagent”, “Lateral Flow” — not “Reader” or “Analyzer”
✅ 3rd-Party Certification (CE, FDA, ISO 13485) ✔️ Prove medical-grade quality
✅ Commercial Invoice ✔️ Use exact HS Code and product name: “Antigen Rapid Test Kit, SARS-CoV-2, Lateral Flow, 25 Tests”
✅ Certificate of Origin (CO) ✔️ If from Vietnam, India, Mexico — may qualify for IEEPA exemption
✅ Packing List ✔️ Show no instrument included

✅ 2.申报 Strategy (Golden Rules)

🔥 “Reagent = 10%, Instrument = 35% — Don’t Mix!”

Scenario Correct HS Code Wrong Code Risk
Test strip + buffer + pipette 3822.19.00.30 or 3002.15.00.91 9027.89.45.30 45% overcharge
Test kit + handheld reader Split申报: Reagent → 3822.19.00.30, Instrument → 9027.89.45.30 Combine into one → 9027.89.45.30 Reagents taxed at 35%
Only test kit (no reader) 3822.19.00.30 9027.89.80.30 35% on reagent

📌 Pro Tip:
- Never call a test kit “analyzer” or “instrument” in the invoice.
- Use “lateral flow test kit”, “antigen detection reagent”, “immunological diagnostic kit”.


✅ 3. Special Cases & Mitigation

Case Solution
Combo kit with reader Split申报: Reagent → 10%, Instrument → 35%
Test kit from Vietnam/Mexico Apply for IEEPA exemption0% duty
Custom-designed kit Submit Advance Ruling Request (ARR) to confirm HS Code
Used for research, not clinical May qualify for non-commercial use exemption (requires proof)

🌍 5. Global Customs Comparison (2026)

Country Recommended HS Code Duty Rate Certification Notes
🇺🇸 USA 3822.19.00.30 10% (if China) FDA, CE, ISO 13485 122条款 applies
🇨🇳 China 3002.14.00.90 5% NMPA No 122条款
🇪🇺 EU 3002.14.00.90 0% (if CE) CE, ISO 13485 No 122条款
🇦🇺 Australia 3002.15.00.91 5% TGA No 122条款
🇯🇵 Japan 3002.14.00.90 0% PMDA No 122条款

📌 Insight:
- Only the U.S. applies 122条款10% on reagents from China.
- Vietnam/Mexico/India products may avoid this — consider shifting production.


📌 6. Common Mistakes & Penalties (Avoid These!)

Mistake 1: Calling a test kit “an analyzer” or “reader”
👉 Result: 35% duty on reagents → massive overpayment

Mistake 2: Including a reader in the same shipment without split申报
👉 Result: Entire shipment taxed at 35% → $100k+ in extra cost

Mistake 3: Not providing reagent composition or test mechanism
👉 Result: Customs delays, audit, or rejection

Mistake 4: Using “diagnostic device” as product name
👉 Result: Misclassified as medical device → 20%+ duty

Correct Labeling Example:

“Antigen Rapid Test Kit, SARS-CoV-2, Lateral Flow, 25 Tests, Reagent-Based, No Instrument Included, CE & ISO 13485 Certified”


🎯 7. Final Verdict: Master the HS Code, Save 25%+

🔹 Reagent-only kit?3822.19.00.3010% duty
🔹 With reader?Split申报 → Reagent: 10%, Instrument: 35%
🔹 No reader?Never use 9027.89.45.30it’s not an instrument!

📣 Pro Tip:
- Apply for Advance Ruling (ARR) if you’re exporting large volumes.
- Shift production to Vietnam/Mexico to avoid 122条款.
- Use a U.S.-based customs broker with experience in medical reagents.


📣 Take Action Now!

📞 Contact a U.S. Customs Broker with medical diagnostics expertise
📄 Request HS Code Pre-Ruling for your ARTK
🚀 Avoid 35% duty traps — declare correctly from Day 1!


Smart Classification = Lower Duty = Higher Profit!
💼 Your product’s value depends on how you declare it — don’t gamble!

用户评价

关于 HS 编码归类

协调制度(HS)是由世界海关组织(WCO)制定的国际贸易商品分类标准。全球 200 多个国家采用 HS 系统作为海关关税、贸易统计和进出口监管的基础。

每个 HS 编码遵循以下层级结构:

  • 章(2 位)——商品大类(例如:第 84 章:机器和机械设备)
  • 品目(4 位)——章内的更具体分类
  • 子目(6 位)——国际通用细分,所有 WCO 成员国统一使用
  • 本国细分(8-10 位)——各国自行扩展的细分编码,如美国 HTSUS 10 位编码

正确的 HS 编码归类对于顺利通关、准确缴纳关税和遵守贸易法规至关重要。错误归类可能导致海关延误、多缴关税或罚款。

CN进口到US时,适用的关税税率可能包括:

  • 最惠国(MFN)税率——适用于 WTO 成员国的标准关税税率
  • 普通税率——适用于无贸易协定国家
  • 贸易救济关税——附加关税,如 301 条款(反倾销)、232 条款(国家安全)或反补贴税

本页内容仅供参考。如需正式归类,请咨询当地海关或持牌报关代理。