Loren Data's SAM Daily™

fbodaily.com
Home Today's SAM Search Archives Numbered Notes CBD Archives Subscribe
FBO DAILY ISSUE OF AUGUST 24, 2012 FBO #3926
SPECIAL NOTICE

99 -- NOTICE OF INTENT TO INCREASE QUANTITIES OF LASER TREATMENT CARDS VIA MODIFICATION TO EXISTING INDEFINITE DELIVERY INDEFINITE QUANTITY (IDIQ) : N626454-11-D-5050

Notice Date
8/22/2012
 
Notice Type
Special Notice
 
NAICS
339115 — Ophthalmic Goods Manufacturing
 
Contracting Office
N62645 Naval Medical Logistics Command 693 Neiman Street Ft. Detrick, MD
 
ZIP Code
00000
 
Solicitation Number
N6264511D5050
 
Archive Date
9/22/2012
 
E-Mail Address
CONTRACT SPECIALIST
(SHAUKAT.MIRZA@MED.NAVY.MIL)
 
Small Business Set-Aside
N/A
 
Description
DEPARTMENT OF THE NAVY NAVAL MEDICAL LOGISTICS COMMAND NOTICE OF INTENET TO SOLE SOURCE The Naval Medical Logistics Command intends to increase the quantities on CLIN 0004 of AMO ™s 10TX “ Addedvue Pak High Myopia Domes, AMO ™s 10TX “ S4 USA LASIK PRK ASTIG and AMOS ™s IFLAP US which are all manufactured by Abbott Medical Optics (AMO) (AMO), 1700 E. St. Andrew Place, Santa Ana, CA 92705, on an existing Indefinite Delivery Indefinite Quantity (IDIQ) : N626454-11-D-5050. The quantity will be increased by 400 units. This procurement will be classified under North American Industry Classification System (NAICS) 339115. Essential Characteristics: The requirement is to add treatment key cards for use with various facilities ™ VISX Photo Refractive Keratectomy (PRK) systems. These PRK systems are used to perform fragile procedures on the eye. Each key card shall provide the proprietary information needed to perform a procedure on the key using the VISX systems mentioned below already located at those facilities. These procedures shall include the following: laser treatment for eye ablation to treat myopia, hyperopia, mixed astigmatism treatment, and high myopia treatment for Lasik; laser treatment for ablation of the surface of the eye; and flap creation for use during Lasik surgical procedures. Regulatory Requirements: The system and all of the components, 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. The system shall be installed in compliance with OSHA requirements. IF YOU CAN SATISFY THIS REQUIREMENT, PLEASE SUBMITT YOUR CAPABILITIES STATEMENTS TO SHAUKAT.MIRZA@MED.NAVY.MIL NO LATER THAN 4:30 ON FRIDAY, 21 SEPTEMBER 2012.
 
Web Link
FBO.gov Permalink
(https://www.fbo.gov/spg/DON/BUMED/N62645/N6264511D5050/listing.html)
 
Record
SN02850081-W 20120824/120823000411-6a218f20a8d8501ae52ee69c92ead77c (fbodaily.com)
 
Source
FedBizOpps Link to This Notice
(may not be valid after Archive Date)

FSG Index  |  This Issue's Index  |  Today's FBO Daily Index Page |
ECGrid: EDI VAN Interconnect ECGridOS: EDI Web Services Interconnect API Government Data Publications CBDDisk Subscribers
 Privacy Policy  Jenny in Wanderland!  © 1994-2024, Loren Data Corp.