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The tariff classification of Oxiplex/SP® Gel
Issued June 6, 2006 by U.S. Customs and Border Protection.
Cite this ruling
Copies to clipboardR0 R04062 (June 6, 2006)
Tariff classification
HTS codes: 3005.90.5090
Headings: 3005
Product description
The subject product, Oxiplex/SP® Gel, is an absorbable adhesion barrier, in the form of a clear, synthetic, sterile gel. The gel is composed of polyethylene oxide and carboxymethylcellulose sodium stabilized with calcium chloride. Oxiplex/SP® Gel is intended to reduce post-surgical epidural adhesions in discectomy, laminectomy, and laminotomy procedures in spine surgery by acting as a temporary mechanical barrier separating opposing tissue surfaces. The gel is put up in a 3mL syringe that, together with a sterile, 5.42”, plastic applicator and instructions for use, is fitted into a sterile, thermoform (plastic) tray. The tray, in turn, is put up packaged for retail sale in a printed box.
CBP rationale
The applicable subheading for the subject product will be 3005.90.5090, Harmonized Tariff Schedule of the United States (HTSUS), which provides for “Wadding, gauze, bandages and similar articles (for example, 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: Other: Other: Other.
Full text
NY R04062 June 6, 2006 CLA-2-30:RR:NC:2:238 R04062 CATEGORY: Classification TARIFF NO.: 3005.90.5090 Ms. Melissa M. Traylor FzioMed, Inc. 231 Bonetti Drive San Luis Obispo, CA 93401 RE: The tariff classification of Oxiplex/SP® Gel Dear Ms. Traylor: In your letter dated May 31, 2006, you requested a tariff classification ruling. The subject product, Oxiplex/SP® Gel, is an absorbable adhesion barrier, in the form of a clear, synthetic, sterile gel. The gel is composed of polyethylene oxide and carboxymethylcellulose sodium stabilized with calcium chloride. Oxiplex/SP® Gel is intended to reduce post-surgical epidural adhesions in discectomy, laminectomy, and laminotomy procedures in spine surgery by acting as a temporary mechanical barrier separating opposing tissue surfaces. The gel is put up in a 3mL syringe that, together with a sterile, 5.42”, plastic applicator and instructions for use, is fitted into a sterile, thermoform (plastic) tray. The tray, in turn, is put up packaged for retail sale in a printed box. The applicable subheading for the subject product will be 3005.90.5090, Harmonized Tariff Schedule of the United States (HTSUS), which provides for “Wadding, gauze, bandages and similar articles (for example, 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: Other: Other: Other.” The rate of duty will be free. Duty rates are provided for your convenience and are subject to change. The text of the most recent HTSUS and the accompanying duty rates are provided on World Wide Web at http://www.usitc.gov/tata/hts/. This merchandise may be subject to the Federal Food, Drug, and Cosmetic Act and/or The Public Health Security and Bioterrorism Preparedness and Response Act of 2002 (The Bioterrorism Act), which are administered by the U.S. Food and Drug Administration (FDA). Information on the Federal Food, Drug, and Cosmetic Act, as well as The Bioterrorism Act, can be obtained by calling the FDA at 1-888-463-6332, or by visiting their website at: www.fda.gov. This ruling is being issued under the provisions of Part 177 of the Customs Regulations (19 C.F.R. 177). A copy of the ruling or the control number indicated above should be provided with the entry documents filed at the time this merchandise is imported. If you have any questions regarding the ruling, contact National Import Specialist Harvey Kuperstein at 646-733-3033. Sincerely, Robert B. Swierupski Director, National Commodity Specialist Division
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