HS Code for Blood Typing Reagents
The HS Code for blood typing reagents is 300620. The MFN duty rate for importing to the US is Free.
| HS Code (6-digit) | 300620 |
|---|---|
| US Duty Rate (MFN) | Free |
| EU Duty Rate (MFN) | 0% |
| Chapter | 30 |
| Heading | 3006 |
| Last Updated | 2026-05 |
Description
Blood-grouping reagents
This HTS code is for blood-grouping reagents used to determine blood types, and they are imported duty-free into the United States.
Frequently Asked Questions
What specific regulatory approvals are required to import blood-grouping reagents under HTS 300620 into the United States?
Imports of blood-grouping reagents are regulated as biological products by the U.S. Food and Drug Administration (FDA) and require a Biologics License Application (BLA) approval. For each shipment, you must provide an FDA Form 356h and the product must be listed with the FDA's Center for Biologics Evaluation and Research (CBER).
What special packaging and shipping conditions are required for blood-grouping reagents under HTS 300620 to ensure product integrity?
Blood-grouping reagents are sensitive diagnostic reagents that typically require temperature-controlled shipping, often between 2°C and 8°C (refrigerated). They must be packaged with sufficient coolant (e.g., gel packs) and insulating material to maintain this range throughout transit, and the outer packaging must be clearly marked "PERISHABLE" and "KEEP COOL" or similar designations. Using a courier with validated cold-chain logistics is essential to prevent degradation and ensure the reagents remain effective for clinical use.
Common Classification Errors for Blood Typing Reagents
A common error is classifying these reagents under heading 3822, which is for other diagnostic reagents. Reagents specifically for determining blood groups or rhesus factors are explicitly provided for in 3006.20. Ensure the product's primary purpose is for blood grouping, not general clinical chemistry testing (e.g., glucose tests under 3822). Products that are combined or sold in kits for broader diagnostic panels must be classified by their individual components, which may split the classification.
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