HS Code for Medical X-Ray Machines
The HS Code for medical x-ray machines is 902214. The MFN duty rate for importing to the US is Free.
| HS Code (6-digit) | 902214 |
|---|---|
| US Duty Rate (MFN) | Free |
| EU Duty Rate (MFN) | 0% |
| Chapter | 90 |
| Heading | 9022 |
| Last Updated | 2026-05 |
Description
Other apparatus based on the use of X-rays, for medical use
HS Code 902214 covers other medical X-ray apparatus, which has a US MFN duty rate of Free.
Frequently Asked Questions
What specific customs inspection risks are associated with importing medical X-ray apparatus under HTS 902214?
Shipments of X-ray machines under HTS 902214 are frequently selected for intensive physical inspection due to the need to verify radiation safety compliance and ensure the apparatus contains no unauthorized dual-use components. Inspectors will typically demand to see detailed technical documentation, including certificates of radiation emission standards from the country of manufacture (e.g., FDA 510(k) for U.S. imports) and proof of intended medical use. Delays are common as inspections often require the presence of a specialist or moving the heavy, sensitive equipment to a designated examination area.
What additional costs beyond the invoice value should I anticipate when importing a medical X-ray apparatus under HTS 902214?
For HTS 902214 apparatus, you must pay a 0% U.S. Most Favored Nation (MFN) duty rate, but you are subject to a 2.7% Medical Device Excise Tax under IRC Section 4191 on the sale price. Furthermore, all imports are subject to a 0.3464% Merchendise Processing Fee (MPF) and a potentially significant Harbor Maintenance Fee (HMF) if arriving by vessel.
Medical X-Ray Machine Compliance Notes
Imports of medical X-ray machines under 9022.14 are subject to strict FDA pre-market notification (510(k)) or pre-market approval (PMA) requirements, and must be listed with the FDA. Shipments typically require an FDA Form 2877. Additionally, all such equipment must comply with the FDA's Radiation Safety Performance Standard (21 CFR Subchapter J, Radiological Health) and electronic product radiation control (EPRC) reporting rules. Importers should verify if state-level radiation control program registration is also required for the end-user facility.
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