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wearable breast pump 2 pack

CN → US

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🤱 Wearable Breast Pump (2-Pack) | The "Hands-Free" Lactation Solution


🌐 HS Code Reference & Customs Clearance Guide | 2026 Latest Tariff Analysis | Professional Level Compliance Strategy
📌 I. Product Definition & Classification: Are You Sure It’s a “Pump” or a “Medical Device”?

A Wearable Breast Pump is a modern, portable lactation aid designed to fit discreetly inside a nursing bra. Unlike traditional plug-in pumps, these are often battery-operated or rechargeable, featuring flexible tubing, collection bottles/bags, and motorized suction mechanisms.

In international trade, the classification hinges on two critical factors: 1. Electrical Component: Does it have a motor/battery? (Yes → Chapter 85) 2. Primary Purpose: Is it a medical device (therapeutic/curative) or a household appliance (general utility)?

⚠️ Key Distinction:
- If marketed as a medical aid for lactation difficulties or postpartum care with specific therapeutic claims → Likely Chapter 90 (Medical Devices).
- If marketed as a general consumer electronic/household appliance for milk collection without specific medical claims → Likely Chapter 85 (Electrical Machinery) or Chapter 84 (Machinery).
- Crucial Note for US Import: The FDA regulates breast pumps as Class II Medical Devices. Misclassification can lead to shipment rejection, even if the HS Code seems plausible.


📦 II. HS Code Classification Details (2026 Latest Tariff Authority Comparison)

HS Code Product Description Applicable Scenario Medical Device Status Electrical Component
8414.59.80 Other vacuum pumps, not for medical use Consumer-grade pumps marketed as "home appliances" ❌ No ✅ Yes (Motor/Battery)
9019.10.00.00 Mechano-therapy appliances; massage apparatus Pumps classified as "mechanical therapy aids" ✅ Yes (FDA Class II) ✅ Yes
9018.19.90.00 Other instruments and appliances used in medical, surgical, dental or veterinary sciences Specific medical lactation pumps with regulatory clearance ✅ Yes (FDA Class II) ✅ Yes
8508.11.00.00 Hand-held vacuum cleaners with electric motor Incorrect – Pumps are not vacuum cleaners ❌ No ✅ Yes
3926.90.97.90 Other articles of plastics Collection bottles/parts only (disassembled) ❌ No ❌ No

🔍 Critical Reminder:
- FDA Regulation: In the US, all breast pumps are Class II Medical Devices. You must have FDA 510(k) clearance.
- Misclassification Risk: Declaring a medical device as a "vacuum cleaner" (8508) or "general appliance" (8414) is a major compliance violation.
- 2-Pack Consideration: The HS Code applies to the unit (one pump). The "2-pack" is just packaging quantity. Do not try to create a new HS Code for the bundle.


💰 III. 2026 Latest Tariff Rate Details (Including Additional Duties)

Applicable Country: United States (US)
Country of Origin: China (CN)
Effective Date: November 10, 2025 onwards (including subsequent imports)

🎯 1. 9019.10.00.00 – Mechano-therapy Appliances (Most Common for Wearable Pumps)

Item Content
Base Duty Rate 0% (ad valorem)
USITC Additional Duty (Section 301) +7.5% (for most medical/electronic goods under specific subheadings)
IEEPA Additional Duty +10% (For China/HK products, effective Nov 10, 2025)
Total Duty Rate 17.5%
Tax Calculation CIF Value × 17.5%
De Minimis Exemption Eligible? No (deny_de_minimis) – Medical devices are exempt from the $800 de minimis rule.
Legal Authority Path IEEPA:9903.01.25IEEPA:9903.01.24USITC:9019.10.00.00FOOTNOTE:9903.88.01

📌 Explanation:
- The 7.5% is a residual Section 301 tariff for many medical/electronic categories.
- The 10% is the new IEEPA tariff added in late 2025.
- Total 17.5% is significantly higher than the 0-2.5% base rate, making cost control essential.

🎯 2. 9018.19.90.00 – Other Medical Instruments

Item Content
Base Duty Rate 0%
USITC Additional Duty (Section 301) +7.5%
IEEPA Additional Duty +10%
Total Duty Rate 17.5%
Tax Calculation CIF Value × 17.5%
De Minimis Exemption Eligible? No

📌 Note:
- Both 9019.10.00.00 and 9018.19.90.00 generally face similar additional duties for Chinese goods.
- Accuracy is Key: If your product is classified under 8414.59.80 (incorrectly), it may face 25% Section 301 + 10% IEEPA = 35%, which is even higher. Always use medical device classifications.


🛠️ IV. Customs Clearance Practical Advice (Real-World Pitfall Guide)

✅ 1. Required Documentation Checklist (Non-Negotiable)

Document Must Provide Description
FDA 510(k) Clearance Number ✔️ Mandatory. Without this, the shipment will be detained at CBP.
Product Specification Sheet ✔️ Must detail suction pressure, battery type, flow rate, and material (BPA-free).
Commercial Invoice ✔️ Must clearly state: "Wearable Breast Pump, Model [XYZ], Medical Device, FDA Cleared".
Certificate of Origin (CO) ✔️ Required for tariff calculations and IEEPA applicability.
Packaging List ✔️ Specify "2-Pack" but declare unit value per pump.
Electrical Compliance ✔️ UL, FCC, or CE certificates (for electrical safety).

✅ 2. Declaration Tips (Critical Keywords)

🔥 "Medical Device First, Electronic Second, Brand and Model Exact!"

Scenario Correct Declaration Wrong Practice
Wearable Pump with Battery HS 9019.10.00.00 "Mechano-therapy appliance, FDA Cleared" "Baby Feeder" or "Milk Extractor" (Vague)
2-Pack Bundle Declare as 2 separate units with combined CIF value Declare as "Set" with one value (CBP may split and audit)
Accessories Only (Bottles) HS 3926.90.97.90 HS 9019.10.00.00 (Misclassification)
Non-Medical "Simulator" HS 8414.59.80 HS 9019.10.00.00 (If not for medical use)

✅ 3. Special Situations

Situation Handling Advice
OEM/ODM Brands Ensure the FDA 510(k) number matches the brand owner or the manufacturer. CBP checks this link.
BPA-Free Certification Provide material safety data sheets. CBP may inspect for hazardous materials compliance.
Battery Type If Lithium-ion, provide UN38.3 Test Summary and MSDS for air/sea freight safety.
"Smart" App-Connected Pumps If the pump has Bluetooth/WiFi, ensure FCC ID is listed. CBP may cross-check electronic compliance.

🌍 V. Global Market Customs Comparison (2026 Latest)

Country/Region Recommended HS Code Tariff Certification Requirements Notes
🇺🇸 USA 9019.10.00.00 17.5% FDA 510(k) + FCC + UL Strict Medical Device Regime. No de minimis.
🇨🇳 China 9019.10.00.00 0% NMPA Registration No additional duties.
🇪🇺 EU 9019.10.00.00 0% MDR (CE Mark) EU Medical Device Regulation (MDR) is stricter than FDA.
🇬🇧 UK 9019.10.00.00 0% UKCA Mark Post-Brexit rules apply.
🇨🇦 Canada 9019.10.00.00 0% Health Canada License Must be licensed for sale.

📌 Conclusion:
- The USA is the most tariff-intensive market for Chinese-made breast pumps due to IEEPA/Section 301.
- Regulatory Compliance (FDA) is more critical than tariff rates. A misdeclared medical device will be seized regardless of low tariffs.


📌 VI. Common Mistakes & Pitfalls (Blood-Teaching Lessons)

Mistake 1: Declaring as "Baby Product" or "Feeding Accessory"
👉 Consequence: CBP reclassifies to medical device + applies penalties + delays shipment.

Mistake 2: Missing FDA 510(k) Number on Invoice
👉 Consequence: Seizure. CBP requires this number to verify medical device status.

Mistake 3: Ignoring Battery Regulations (UN38.3)
👉 Consequence: Carrier refusal (FedEx/UPS/DHL will reject lithium battery shipments without proper documentation).

Mistake 4: Under-declaring Value in a 2-Pack
👉 Consequence: CBP may value each pump separately, leading to higher duties and potential fraud allegations.

Correct Declaration Example:

"Wearable Breast Pump, Model XYZ, 2-Pack, Rechargeable, BPA-Free, FDA Cleared (510(k) #K230000), HS Code: 9019.10.00.00"


🎯 VII. Conclusion: Professional Compliance Saves Costs!

🎯 Remember:

🔹 "Medical Device First, FDA Number Must!"
🔹 "No De Minimis for Med Devices, Think Before You Ship!"
🔹 "Lithium Battery Needs UN38.3, Or Carrier Will Stop!"


📌 Pro Tip:
If your pumps are manufactured in Vietnam or Malaysia, you may avoid the 10% IEEPA tariff and potentially reduce Section 301 duties. Consider supply chain diversification to lower landed costs.


📣 Immediate Action:

📞 Verify FDA 510(k) Clearance before shipping.
📦 Ensure UN38.3 & MSDS for lithium batteries.
📝 Use HS Code 9019.10.00.00 for accurate duty calculation.
🚀 Protect your brand with compliance, not just cost-cutting!


Professional Customs Clearance, Starting with Accurate Classification!
💼 Your Product’s Safety and Legality Are Your Best Marketing!

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。