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Product Overview The dental kit classified under HS Code 901849 encompasses a range of portable assemblies containing dental instruments and accessories designed for professional oral healthcare applications. These kits typically include tools such as dental mirrors, probes, scalers, forceps, and occasionally handpieces or small sterilization components, consolidated in a single, organized case. The physical specifications vary but generally feature stainless steel instruments with corrosion-resistant properties, precision-engineered tips, and ergonomic handles to ensure durability and clinical efficacy. Processing levels range from sterilized, ready-to-use sets to non-sterile kits intended for subsequent sterilization. Within HS Code 901849, subcategories include dental instruments for surgery, examination, and cleaning, each differentiated by function and material composition. Commercially, these dental kits are integral to dental practices, mobile clinics, and educational institutions, facilitating procedures in preventive, diagnostic, and therapeutic dentistry. Their market positioning hinges on quality assurance, compliance with medical standards, and adaptability for international regulatory environments, providing importers and distributors with reliable, standardized product offerings suitable for diverse healthcare markets. HS Code Classification & Trade Specifications The dental kit falls under the HS Code 901849, structured hierarchically as follows: Chapter 90 (Optical, photographic, cinematographic, measuring, checking, precision, medical or surgical instruments and apparatus), Heading 9018 (Instruments and appliances used in medical, surgical, dental or veterinary sciences), and Subheading 901849 (Dental instruments, including dental drills and other rotary instruments). This classification is warranted due to the kit’s composition of specialized dental instruments designed explicitly for clinical use, aligning with international HS nomenclature. Trade considerations emphasize packaging that ensures contamination prevention and mechanical protection, typically vacuum-sealed or contained within rigid, impact-resistant cases to maintain instrument integrity during transit. Preservation methods focus on sterility maintenance where applicable, adhering to ISO 17665 or equivalent sterilization standards. Shipping requirements mandate compliance with international regulations on medical devices, including proper labeling, documentation for customs clearance, and adherence to WTO trade facilitation measures. Quality standards encompass conformity with ISO 13485 for medical device manufacturing and relevant CE or FDA certifications, ensuring global acceptance and mitigating import/export compliance risks. This precise classification supports efficient customs processing and facilitates accurate tariff application in international trade operations.