RSV Fusion Protein Antigen Test
A monoclonal antibody-based capture test for detecting Respiratory Syncytial Virus (RSV) fusion protein antigens in nasal wash specimens. The test uses a membrane backing with immobilized antibodies and is a prepared diagnostic reagent for pediatric respiratory infections. It is not a medicament and is classified as a diagnostic laboratory reagent.
Import Duty Rates by Country of Origin
| Origin Country | MFN Tariff | Surtaxes | Total Effective Rate |
|---|---|---|---|
| π¨π³China | Free | β | Free |
| π²π½Mexico | Free | β | Free |
| πΊπΈUnited States | Free | β | Free |
| π©πͺGermany | Free | β | Free |
| π―π΅Japan | Free | β | Free |
Alternative Classifications
This product could be classified differently depending on its characteristics or intended use.
If the test is for malaria detection
Subheading 3822.11 is specific to malaria diagnostic kits.
If the product is a monoclonal antibody for therapeutic administration
Therapeutic monoclonal antibodies are classified in heading 30.02, not as diagnostic reagents.
Not sure which classification is right?
The Tariff Assistant works through the GRI rules on your specific product to reach the right tariff item β and can price the duty on it in the same conversation.
Import Tips & Compliance
β’ Check if the test is classified as a Class III medical device under Health Canada's regulations, as this affects import requirements
β’ Provide a letter of attestation that the product is for diagnostic, not therapeutic, use
β’ Keep a copy of the device licence or import authorization with your customs documents
Related Products under Tariff item 3822.19.00
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