134 VeinViewer Vision2 User Guide 020-101077-05 Rev. 1 (02-2016) ITEM NUMBER DESCRIPTION OF SUPPLIES/SERVICES QUANTITY UNIT UNIT PRICE AMOUNT 0001 2.00 EA $0.00 $0.00 VEIN VIEWER VISION2 WITH MAX REACH HEAD TO TOE IMAGING WITH 5 YEAR WARRANTY. LOCAL STOCK NUMBER: 134-003104-01 GRAND TOTAL $0.00 This Sources Sought Notice is for informational and planning purposes only and shall not be construed as a solicitation or as an obligation or commitment by the Government. This notice is intended strictly for market research. The purpose of this Sources Sought notice is to determine interest and capability of businesses including (but not limited to) 8(a), HUBZone, Service Disabled Veteran-Owned Small Business, and Veteran-Owned Small Business firms relative to the North American Industry Classification Code (NAICS) 336112. The Department of Veterans Affairs is seeking both manufacturers and/or distributors of the exact match or functionally equivalent equipment/ services to the following listed above with a suspense date of Tuesday, 06/11/2019 at 3pm CST. Nursing Vien viewer - Statement of Work (SOW) Project Description: To purchase Vein Viewer to support new infusion clinic and inpatient med surg unit. Specifications: Viewer: Weight (assembled device) Not to exceed 54 lbs Height (assembled device) Not to exceed 69.8 in Basket Weight Limit Hold a minuim of 0.5 lbs Power Rating Input (AC Mains): 100-240 VAC, 50/60 Hz, 25W, 0.45A at 115VAC typical and 0.3A at 230VAC typical Input (Battery): 9V DC, 1.42A Maximum Equipment Protection Class: Class II (AC Power Cord) Battery Rechargeable Battery Pack IR Wavelength, peak Approximately 850 nm Visible Wavelength, peak Amber LED: 617 nm Green LED: Approximately 525 nm Blue LED: 465 nm Technical Specifications Battery Duty Cycle Continuous Operating Temperature +60°F to +86°F (+16°C to +30°C) Storage Temperature -10°F to +140°F (-23°C to +60°C) Storage Humidity 0% to 90% non-condensing Atmospheric Pressure (storage and operating) 700 hPa to 1,060 hPa Humidity (storage and operating) 10% to 90% non-condensing Safety Has been tested to and complies with General Requirements for Safety per IEC 60601-1. Compliant with IEC 60601-1 National differences for: Austria, Belgium, Canada, Switzerland, Czech Republic, Germany, Denmark, Finland, France, United Kingdom, Hungary, Israel, Italy, Japan, Netherlands, Norway, Poland, Sweden, Singapore, Slovakia, Slovenia, Turkey, Ukraine, United States. Emission Has been tested to and complies with IEC60601-1-2 standard for Electromagnetic Compatibility (EMC) and for radiated and conducted emissions. EMC Classified A Regulatory Classified FDA Class 1 Exempt LED Radiation Class 1 LED Product as per IEC 60825-1 ED. 1.2 (2001) LED maximum output: 523nm (A1) = 1.60 mW 875nm (A2) = 1.778mW Equipment Classification classification as a medical device. Class II or Internally Powered Equipment. Protection Against Ingress of Liquids - Ordinary. Mode of operation of equipment - Continuous Operation. Stand: Wheeled stand for hands-free use of Vein viewer. Minuin 5 prong/leg base for stand s stable base and smooth gliding wheels. Arm, to allow for vien viewer to be precisely positioned to keep the selected vein highlighted. Arm extended and flexible reach must allow the patient can be easily accessed with User and Service Manuals: The vendor shall provide a complete printed sets as well as electronic version of operator manuals, service manuals, electronic schematics, troubleshooting guides and parts list for each bladder scan purchased for each medical center. These manuals will include all components and subassemblies, including those not manufactured by the vendor. Provide a manual or reference guide for how equipment should be cleaned and disinfected. Information System Officer, Information Protection: The contractor will not have access to VA Desktop computers they will not have access to online resources belonging to the government. Privacy Officer: The Contractor will not have access to protected Patient Health Information (PHI) nor will they have capability of accessing patient information during the services provided to the VA and if removal of equipment from the VA is required, any memory storage device will remain in VA control and will not be removed from VA custody. All research data available for Contractor analysis is de-identified. Records Manager: Records Manager:  There will not be federal records created, maintained, used or dispositioned with this contract;  regardless of format [paper, electronic, etc.] or mode of transmission [e-mail, fax, etc.]

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