Medical Device Calibration Pump
Infusion pump exported to European hospital, returned temporarily to US for annual calibration and firmware update. Qualifies under 9801.00.10.12 for temporary repair/alteration of US medical equipment to be reexported within 3 years.
Import Duty Rates by Country of Origin
Alternative Classifications
This product could be classified differently depending on its characteristics or intended use.
If entered as new medical instruments
Standard classification for infusion pumps with full import duties
If >3 years since export
Permanent US goods return provision without time limit
If for repair components only
Institutional equipment repair parts; different subchapter scope
Not sure which classification is right?
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Import Tips & Compliance
• Include FDA 510(k) clearance docs and calibration certificates proving no design changes,Temporary import bond may be required; ensure service records show reexport plan,Avoid pitfall of permanent import classification by documenting original export
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