HS subheading 9021 39 Other
HS subheading 9021 39 covers other (Orthopaedic appliances, including crutches, surgical belts and trusses; splints and other fracture appliances; artificial parts of the body; hearing aids and other appliances which are worn or carried, or implanted in the body, to compensate for a defect or disability).
- EUDR
- Not in scope
- Level
- HS subheading
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Describe the product in your own words and Klassio suggests a CN code with reasoning, duty and EUDR status.
Importing into the EU
Codes under 9021 39
Goods that have been classified here
Examples from the EU database of Binding Tariff Information (BTI). A ruling binds only its holder and many have expired — read them as guidance, not as a decision for your product.
IOL (INTRA OCULAR LENS) THIS IS AN ARTIFICIAL LENS IMPLANTED IN THE EYE OF AN ADULT PATIENT TO CORRECT VISION AFTER HAVING THE LENS REMOVED DUE TO A CATARACT.
ORTHOPAEDIC IMPLANT (SPINE DISC) MADE FROM COBALT CHROME (COCR) ALLOY USED TO COMPENSATE FOR DEFECT/DISABILITY.
IOL (INTRA OCULAR LENS) USED TO REPLACE THE HUMAN LENS TO CURE CATARACTS.THIS IS AN OPTICAL IMPLANT
VASCULAR ACCESS IMPLANT DEVICE. THE PRODUCT IS AN ARTERIAL GRAFT COMPONENT WHICH COMPRISES OF AN EPTFE GRAFT, WHICH IS PLACED SUBCUTANEOUSLY BY AN ARTERIAL ANASTOMOSIS AND TUNNELLED TO THE DELTOPECTORAL GROOVE AND CONNECTED TO THE OUTFLOW COMPONENT. THE IMPLANT IS USED FOR END STAGE RENAL DISEASE PATIENTS ON HAEMODIALYSIS, WHO HAVE EXHAUSTED ALL OTHER ACCESS OPTIONS.
VASCULAR ACCESS DEVICE. THE PRODUCT IS A VENOUS OUTFLOW COMPONENT WHICH COMPRISES OF A BRAIDED NITONOL TUBE WITH A SILICONE COATING. THE TUBE IS SURGICALLY IMPLANTED IN THE BODY THROUGH THE INTERNAL JUGULAR, FOR END STAGE RENAL DISEASE PATIENTS ON HAEMODIALYSIS, WHO HAVE EXHAUSTED ALL OTHER ACCESS OPTIONS.
NON STERILE SURGICAL SUTURE MADE OF 100% SPECTRA. THE SPECTRA IS BRAIDED. WITH A TITANIUM BUTTON ATTACHED TO THE SUTURE. IT IS SURGICALLY IMPLANTED AND REMAINS IN THE PATIENT.
A MADE-UP NON-STERILE, UNCOATED FIBRE WIRE SURGICAL SUTURE MADE OF POLYETHYLENE FIBRE AND POLYESTER, WHERE THE POLYETHYLENE PREDOMINATES. THE MATERIAL IS BRAIDED. WITH A TITANIUM BUTTON ATTACHED TO THE SUTURE. IT IS SURGICALLY IMPLANTED AND REMAINS IN THE PATIENT.
A MADE-UP NON-STERILE, UNCOATED FIBRE WIRE SURGICAL SUTURE LOOP MADE OF POLYETHYLENE FIBRE AND POLYESTER, WHERE THE POLYETHYLENE PREDOMINATES. THE MATERIAL IS BRAIDED. WITH A TITANIUM BUTTON ATTACHED TO THE SUTURE LOOP. IT IS SURGICALLY IMPLANTED AND REMAINS IN THE PATIENT.
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Describe the product in your own words and Klassio suggests a CN code with reasoning, duty and EUDR status.