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 / 3002.14.00.90 → 10% total
- Instrument + test kit combo (e.g., reader + cassette) → 9027.89.45.30 / 9027.89.80.30 → 35% 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:9903.01.25 → 122条款:3822.19.00.30 → FOOTNOTE: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:9901.25 → 122条款:3002.15.00.91 → FOOTNOTE: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:9903.01.24 → 122条款:3002.14.00.90 → FOOTNOTE:9903.88.01 |
📌 Why 10%?
- The product is a reagent used in immune reactions — not 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:9903.01.25 → USITC:9027.89.45.30 → 122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 high — avoid 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:9903.01.24 → USITC:9027.89.80.30 → 122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 exemption → 0% 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? →
3822.19.00.30→ 10% duty
🔹 With reader? → Split申报 → Reagent: 10%, Instrument: 35%
🔹 No reader? → Never use 9027.89.45.30 — it’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!
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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。
从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。