Kinesiology tape Hs Code

Kinesiology tape harmonized system code

Product Overview Kinesiology tape, classified under HS Code 300510, is a medical adhesive tape designed to support muscles and joints by enhancing circulation and proprioception. This product is comprised of elastic cotton fabric with acrylic adhesive, engineered for skin compatibility and durability. It typically measures 5 cm in width and 5 m in length per roll, with elasticity ranging from 130% to 160% of its original length, ensuring flexibility and conformability during physical activity. The tape undergoes sterilization and quality assurance processes to meet medical-grade standards, including biocompatibility and hypoallergenic certifications. Within the HS Code 300510 category—which broadly covers adhesive dressings and similar articles—kinesiology tape is distinguished by its elastic properties and therapeutic application, as opposed to rigid or purely protective tapes. Commercially, it is utilized extensively in sports medicine, physiotherapy, and rehabilitation sectors, as well as by retail pharmacies and healthcare providers. Its market positioning is underscored by reliable performance, standardized manufacturing, and compliance with international medical device regulations, offering importers and distributors a consistent and verifiable product for therapeutic use. HS Code Classification & Trade Specifications The complete HS Code for kinesiology tape is 3005.10, situated within Chapter 30: Pharmaceutical Products, Heading 3005: “Wadding, gauze, bandages and similar articles (e.g., dressings, adhesive plasters, poultices), impregnated or coated with pharmaceutical substances or put up in forms or packings for retail sale for medical, surgical, dental or veterinary purposes,” and Subheading 300510: “Adhesive dressings and other articles having a layer of adhesive, for medical, surgical, dental or veterinary purposes.” This classification is justified based on the product’s composition—elastic fabric with adhesive layer—and its intended medical use. Trade considerations include packaging in sterile, moisture-resistant pouches, often in batches of 10 to 20 rolls per carton, to maintain product integrity during transit. Preservation methods focus on preventing contamination and adhesive degradation, with shipping typically requiring ambient temperature control and compliance with International Air Transport Association (IATA) and International Maritime Organization (IMO) regulations. Quality standards align with ISO 13485 for medical devices, and products must conform to WTO Technical Barriers to Trade (TBT) Agreement requirements, ensuring harmonized customs declarations and facilitating smooth clearance across global markets.

Kinesiology tape Chapter Note

1.- This Chapter does not cover : (a) Foods or beverages (such as dietetic, diabetic or fortified foods, food supplements, tonic beverages and mineral waters), other than nutritional preparations for intravenous administration (Section IV); (b) Products, such as tablets, chewing gum or patches (transdermal systems), containing nicotine and intended to assist tobacco use cessation (heading 24.04); (c) Plasters specially calcined or finely ground for use in dentistry (heading 25.20); (d) Aqueous distillates or aqueous solutions of essential oils, suitable for medicinal uses (heading 33.01); (e) Preparations of headings 33.03 to 33.07, even if they have therapeutic or prophylactic properties; (f) Soap or other products of heading 34.01 containing added medicaments; (g) Preparations with a basis of plaster for use in dentistry (heading 34.07); (h) Blood albumin not prepared for therapeutic or prophylactic uses (heading 35.02); or (ij) Diagnostic reagents of heading 38.22. 2.- For the purposes of heading 30.02, the expression “immunological products” applies to peptides and proteins (other than goods of heading 29.37) which are directly involved in the regulation of immunological processes, such as monoclonal antibodies (MAB), antibody fragments, antibody conjugates and antibody fragment conjugates, interleukins, interferons (IFN), chemokines and certain tumor necrosis factors (TNF), growth factors (GF), hematopoietins and colony stimulating factors (CSF). 3.- For the purposes of headings 30.03 and 30.04 and of Note 4 (d) to this Chapter, the following are to be treated : (a) As unmixed products : (1) Unmixed products dissolved in water; (2) All goods of Chapter 28 or 29; and (3) Simple vegetable extracts of heading 13.02, merely standardised or dissolved in any solvent; (b) As products which have been mixed : (1) Colloidal solutions and suspensions (other than colloidal sulphur); (2) Vegetable extracts obtained by the treatment of mixtures of vegetable materials; and (3) Salts and concentrates obtained by evaporating natural mineral waters. 4.- Heading 30.06 applies only to the following, which are to be classified in that heading and in no other heading of the Nomenclature : (a) Sterile surgical catgut, similar sterile suture materials (including sterile absorbable surgical or dental yarns) and sterile tissue adhesives for surgical wound closure; (b) Sterile laminaria and sterile laminaria tents; (c) Sterile absorbable surgical or dental haemostatics; sterile surgical or dental adhesion barriers, whether or not absorbable; (d) Opacifying preparations for X-ray examinations and diagnostic reagents designed to be administered to the patient, being unmixed products put up in measured doses or products consisting of two or more ingredients which have been mixed together for such uses; (e) Placebos and blinded (or double-blinded) clinical trial kits for use in recognised clinical trials, put up in measured doses, even if they might contain active medicaments; (f) Dental cements and other dental fillings; bone reconstruction cements; (g) First-aid boxes and kits;(h) Chemical contraceptive preparations based on hormones, on other products of heading 29.37 or on spermicides; (ij) Gel preparations designed to be used in human or veterinary medicine as a lubricant for parts of the body for surgical operations or physical examinations or as a coupling agent between the body and medical instruments; (k) Waste pharmaceuticals, that is, pharmaceutical products which are unfit for their original intended purpose due to, for example, expiry of shelf life; and (l) Appliances identifiable for ostomy use, that is, colostomy, ileostomy and urostomy pouches cut to shape and their adhesive wafers or faceplates.