Attachment 3: Gray Market and Counterfeit Items
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A PDF document (88 KB) attached to Dentrix Enterprise, Electronic Dental Record (EDR) Services and Support, from the Indian Health Service. Due Nov 10, 2026, 5:00 PM (UTC-7).
File name: Attachment 3_Gray Market and Counterfeit Items_.pdf
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10/22/26, 9:11 AM
852.212-71 Gray Market and Counterfeit Items.
852.212-71 Gray Market and Counterfeit Items.
As prescribed in 812.301(f), insert the following clause: Gray Market and Counterfeit Items (FEB 2023)
(a) No used, refurbished, or remanufactured supplies or equipment/parts shall be provided. This procurement is for new Original Equipment Manufacturer (OEM) items only. No gray market items shall be provided. Gray market items are OEM goods intentionally or unintentionally sold outside an authorized sales territory or sold by non-authorized dealers in an authorized sales territory. (b) No counterfeit supplies or equipment/parts shall be provided. Counterfeit items include unlawful or unauthorized reproductions, substitutions, or alterations that have been mismarked, misidentified, or otherwise misrepresented to be an authentic, unmodified item from the original manufacturer, or a source with the express written authority of the original manufacturer or current design activity, including an authorized aftermarket manufacturer. Unlawful or unauthorized substitutions include used items represented as new, or the false identification of grade, serial number, lot number, date code, or performance characteristics. (c) Vendor shall be an OEM, authorized dealer, authorized distributor, or authorized reseller for the proposed equipment/system, verified by an authorization letter or other documents from the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions.
(End of clause)
Parent topic: Subpart 852.2—Text of Provisions and Clauses
https://www.acquisition.gov/node/64447/printable/print
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