The Naval Medical Logistics Command intends to negotiate on a sole source basis IAW FAR 13.501 with KLS Martin P.O. Box 16369 Jacksonville, FL 32245 as the only responsible source that can provide a Dental Electric Surgical Handpiece Systems in accordance with the Authorized Medical Allowance List (AMAL) for a particular class of ships. In compliance with the Command’s initiative to enhance Integrated Logistic Support (ILS) for Fleet applications, the only technically acceptable item that has (ILS) support is the Sequential Compression Devices is manufactured by Bien Air and distributed by KLS Martin. FAR 13.106 under the authority of the only one responsible source and no other supplies or services will satisfy agency requirements. There are no set-aside restrictions for this requirement. The intended procurement will be classified under North America Industry Classification System (NAICS) 339114 with a Small Business Size Standard of 500. This notice of intent is not a request for competitive proposals and no solicitation document exists for this requirement. BIEN AIR, CHIROPRO 980-1 MOTOR 1 CABLE/1 FOOT SWITCH/1 MOTOR/ 1 CONSOLE BIEN AIR, PMAM 1221 STRAIGHT HANDPIECE, 1:2 RATIO, FOR 45MM BURR, W/ IRRIGATION TUBE Bien Air, CA 30121 Contra Angled Handpiece, 30x Reducer BIEN AIR, LUBRIFLUID, 500ML CAN, LUBRICANT FOR DRILLS BIEN AIR, SPRAYNET, 500ML CAN, CLEANING SPRAY FOR DRILLS CARBIDE BUR, #703, 2.1MM HEAD #2 SHANK (51MM LENGTH),10/PKG, STERILE, SINGLE USE ONLY Carbide Bur, #702, 1.6mm Head, #1 Shank (44.5mm length), Non-Sterile, Single Use Only, 10/Pkg Carbide Bur, #701, 1.2mm Head, #1 Shank (44.5mm length), Non-Sterile, Single Use Only, 10/Pkg BIEN AIR MAINTANENCE AND SERVICE PLAN All equipment and accessories shall be new from the manufacturer. Used or refurbished equipment, or equipment obtained from a third party shall not be accepted. Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. However, parties interested in responding to this notice will need to submit technical data, including cost, sufficient to determine capability in providing the same product. All capability statements received by the closing date of this synopsis will be considered by the Government. A determination by the Government not to compete based on responses to this notice is solely within the discretion of the Government. Information received will be considered solely for the purpose of determining whether to conduct a competitive procurement. Capability statements shall be submitted by email only as a MS Word or Adobe PDF attachment to Jaime Belletto,
[email protected] by 4 PM EST on August 17, 2011. No phone calls accepted.