Federal Bid

Last Updated on 20 Mar 2009 at 8 AM
Solicitation
Frederick Maryland

ALCON CONSTELLATION W/ LASER

Solicitation ID N6264509RCES078
Posted Date 19 Feb 2009 at 1 PM
Archive Date 20 Mar 2009 at 5 AM
NAICS Category
Product Service Code
Set Aside No Set-Aside Used
Contracting Office Not Specified
Agency Department Of Defense
Location Frederick Maryland United states 21702
The Naval Medical Logistics Command intends to negotiate on a sole source basis (IAW FAR 13.5) with Alcon Laboratories, Inc., 6201 South Freeway, Fort Worth, TX 76134, as the only responsible source that is capable of providing an Alcon Constellation System with Laser. Specifically, the requirement is for a vitrectomy system. The system shall be a multi-function ophthalmic surgical system for the anterior and posterior segments of the eye. The system shall be used for vitreoretinal surgeries such as the treatment of retinal detachment, intraocular tumors, severe eye trauma, and the ocular disorders associated as complications of diabetes and sickle cell disease. The system shall be capable of supporting a minimum of 4,000 cuts per minute. The system shall have an integrated 532nm green laser with the full function operability of a traditional ophthalmic microsurgical system. The system shall also have an integrated xenon light source and have at least a 23 gauge probe. The system must have an intraocular pressure control system and footswitch to give the operator hands-free control of multiple functions. The system shall easily transition between the various devices/tools commonly used in vitrectomy and cataract cases. Alcon Laboratories is the only acceptable manufacturer that can provide a vitrectomy system that meets the minimum cutting speed requirement that also has an integrated ophthalmic green laser. The system shall be compliant with the Food and 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. This acquisition is being conducted under simplified acquisition procedures (IAW FAR 13.5). There are no set-aside restrictions for this requirement. The intended procurement will be classified under North American Industry Classification System (NAICS) 339115 with a Small Business Size Standard of 500 employees. This notice of intent is not a request for competitive proposals and no solicitation document exists for this requirement. However, parties interested in responding to this notice will need to submit technical data sufficient to determine capability in providing the same product. Due to the urgency of this requirement, all capability statements received within 15 days after publication 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 normally 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 James Suerdieck at [email protected]. Statements are due by COB 05 MAR 2009. No phone calls accepted.
Bid Protests Not Available

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