HS 30.02
HeadingHuman blood; animal blood for therapeutic, prophylactic or diagnostic uses; antisera, other blood fractions, immunological products, modified or obtained by biotechnological processes; vaccines, toxins, cultures of micro-organisms (excluding yeasts) etc
HS Code 30.02 classifies "Human blood, animal blood for therapeutic, prophylactic or diagnostic uses, antisera, other blood fractions, immunological products, modified or obtained by biotechnological processes, vaccines, toxins, cultures of micro-organisms (excluding yeasts) etc" under Section VI (Products of Chemical or Allied Industries). This heading-level code is used internationally for customs classification, tariff determination, and trade statistics.
Classification Details
πΊπΈ US Import Duty
Rates are approximate and based on MFN (Most Favored Nation) tariffs. Actual rates may vary by specific product classification. Always verify with USITC for official rates.
Classification Guide
When classifying goods under HS 30.02, ensure the product matches the specific description. This is a heading-level code. For customs declaration, you may need the more specific 6-digit subheading. Check with your national customs authority for additional digits required.
Trade Context
Section VI covers chemical and pharmaceutical products β a high-value trade sector.
Regulatory Note
Pharmaceutical imports often require regulatory approval (FDA, EMA). Chemical safety data sheets (SDS) are mandatory for most products.
πΊπΈ US Import Document Checklist
Documents required when importing products under HS 30.02 into the United States.
Required for All Imports
βCommercial InvoiceCBP
βPacking ListCBP
βBill of Lading (B/L) or Airway BillCarrier
βCBP Entry Summary (Form 7501)CBP
βImporter Security Filing (ISF/10+2)CBP
βCustoms BondCBP
Product-Specific Requirements
β οΈFDA Drug RegistrationRequired
Drug establishments must be registered with FDA. Foreign manufacturers need a US Agent.
Agency: FDA
β οΈFDA Drug ListingRequired
All commercially marketed drugs must be listed with the FDA.
Agency: FDA
πDEA Import PermitMay be required
Required for controlled substances (Schedule I-V). Apply at least 4 weeks before import.
Agency: DEA
πCertificate of Pharmaceutical Product (CPP)May be required
WHO-format certificate confirming the product is authorized in the country of origin.
Agency: FDA
FTA Certificate of Origin (for preferential rates)
This checklist is for general guidance only. Actual requirements may vary based on specific product, country of origin, and current regulations. Always consult with a licensed customs broker or the relevant agency for official requirements.