Loren Data's SAM Daily™

FBO DAILY - FEDBIZOPPS ISSUE OF MAY 26, 2018 FBO #6028
DOCUMENT

66 -- Ophthalmic Laser Precision Laser System - Catalyst-U Catalyst System - Attachment

Notice Date

5/24/2018
 

Notice Type

Attachment
 

NAICS

333314 — Optical Instrument and Lens Manufacturing
 

Contracting Office

ALEXANDRIA VA HEALTH CARE SYSTEM;NETWORK CONTRACTING OFFICE 16;ALEXANDRIA VA HEALTH CARE SYSTEM;PO BOX 69004;ALEXANDRIA LA 71306-9004
 

ZIP Code

71306-9004
 

Solicitation Number

36C25618Q9448
 

Response Due

5/31/2018
 

Archive Date

7/30/2018
 

Point of Contact

Arlene Blade
 

E-Mail Address

466-4281<br
 

Small Business Set-Aside

N/A
 

Description

The Department of Veterans Affairs Medical Center, NCO 16 Network Contracting Office, on behalf of the Gulf Coast Veterans Health Care System is conducting market research through this sources sought notice to seek sources to identify potential experienced businesses that are capable of meeting the requirements per the specifications of items listed below. The North American Industry Classification System (NAICS) Code for this acquisition is 333314. Disclaimer and Important Notes: This Sources Sought Notice is for market research purposes only and does not constitute a Request for Proposal/Quotation; and, it is not considered to be a commitment by the Government to award a contract nor will the Government pay for any information provided; no basis for claim against the Government shall arise as a result from a response to this Sources Sought Notice or Government use of any information provided. Failure to submit information in sufficient detail may result in considering a company as not a viable source and may influence competition and set-aside decisions. Regardless of the information obtained from this Sources Sought Notice, the Government reserves the right to consider any arrangement as deemed appropriated for this requirement. Respondents are advised that the Government is under no obligation to acknowledge receipt of the information received or provide feedback to respondents with respect to any information submitted. No proprietary, classified, confidential, or sensitive information should be included in your response to this Sources Sought Notice. The Government reserves the right to use any information provided by respondents for any purpose deemed necessary and legally appropriate, including using technical information provided by respondents in any resultant solicitation. At this time no solicitation exists; therefore, Do Not Request a Copy of the Solicitation. After a review of the responses received, a solicitation may be published on Federal Business Opportunities FedBizOpps website. It is the potential offeror's responsibility to monitor FedBizOpps for release of any future solicitation that may result from this Sources Sought Notice. However, responses to this Sources Sought Notice will not be considered adequate responses to any resultant solicitation. Pursuant to FAR Part 10 (Market Research), the purpose of this notice is to: (1) determine if sources capable of satisfying the agency's requirements exists, (2) determine if commercial items suitable to meet the agency's needs are available or could be modified to meet the agency's requirements, and (3) determine the commercial practices of company's engaged in providing the needed service or supply. Pursuant to FAR Part 6 and FAR Part 19, competition and set-aside decisions may be based on the results of this market research. This notice in no way obligates the Government to any further action. SAM: Interested parties should register in the SAM as prescribed in FAR Clause 52.232-33. The SAM can be obtained by accessing the internet at www.sam.gov. Submission of Information: Companies having capabilities necessary to meet or exceed the stated requirements are invited to provide information to contribute to this market survey/sources sought notice including commercial market information and company information. Companies may respond to this Sources Sought Notice via e-mail to arlene.blade@va.gov no later than May 31, 2018 at 1:00 PM, Central Time. Fax or Telephone calls will not be accepted. Your response should include both the STATEMENT OF CABABILITY and BUSINESS SIZE AND SOCIO-ECONOMIC STATUS information as explained above. Please place "Attention: 36C25618Q9448 Ophthalmic Laser System in the subject line of your response. Please submit the following: 1. Name of Company, Address and DUNS Number. 2. Point of Contact and Phone Number. 3. Business Size applicable to the NAICS Code: a. HuBZone Small Business ; b. Service-Disabled Veteran Owned Small Business (SDVOSB); c. Veteran Owned Small Business (VOSB); d Small Business; e. Large Business 4. Documentation Verifying Small Business Certification: a. If claiming HuBZone status, provide a copy of your HuBZone Certificate from SBA. b. If claiming SDVOSB/VOSB status, provide documentation that shows the business is VetBiz certified. d. If claiming Small Business status, provide documentation to show the business is small under NAICS code 333314. e. Submit a brief description, five (5) pages or less, that demonstrates how your company has the supervision, facilities, labor and experience to provide the Equipment (new equipment only) as described below. f. Documentation to indicate the vendor is an Original Equipment Manufacturer (OEM), authorized delaer, authorized distributor or authorized reseller for the proposed equipment. REQUIREMENT SPECIFICATIONS: Cataract Femtolaser System 1 each EQUIVALENT TO: Abbott Medical Optics/ Catalysis-U Specifications/Salient Characteristics: System must be capable of complete segmentation and softening of cataracts utilizing adjustable grid sizing Device must be capable of preforming at a minimum the following Capsulotomy Lens fragmentation Corneal Arcuate Incision Corneal Primary Incisions and Side-ports Capable of performing capsulotomies within 30 m Device must have 3D Optical Coherence Tomography capabilities Must be capable of performing automated surface mapping algorithms that are utilized to guide the laser Device must come with an integrated patient chair that is height adjustable and utilizes a joystick for x, y movement. The chair must have at a minimum two locking mechanisms Device must be capable of performing femtosecond laser operations utilizing at a minimum the following parameters At-least a 1030nm wavelength A pulse duration of <600 fs At a minimum a pulse repetition rate of 120kHz A pulse energy range at a minimum of 3-10 Microjoules Device must have an optical coherence tomography system with at a minimum the following specifications 3D spectral domain Wavelength range of at a minimum of 820-930nm Resolution rate at a minimum of Axial 30 Microjoules Lateral 15 Microjoule The device must also have a video system that is capable of 40 Microjoule lateral resolution with at a minimum of a 17mm field of view as well as streaming video Liquid Optics Interface: 60 boxes of 20 EQUIVALENT TO: Abbott Medical Optics/ LOI-BP Specifications/Salient Characteristics: Must be compatible with Cataract Femtolaser System Must have the ability to be utilized with patients with glaucoma Must be able to provide a clear path for corneal incisions Must provide a non-applanating interface design Must allow for personalization of surgical procedures Must be capable of providing a stable Intraocular pressure Must minimize the occurrence of corneal folds Must be sterile Must be for single patient utilization Must be capable of centering and fixating the patients eye to the system Utilize an annular ring or equivalent mechanism to apply suction to the patients eye 14.5mm Liquid Optics Interface - 20 boxes of 20 EQUIVALENT TO: Abbott Medical Optics/ LOI-12-BP Specifications/Salient Characteristics: Must be compatible with Cataract Femtolaser System Must have the ability to be utilized with patients with glaucoma Must be able to provide a clear path for corneal incisions Must provide a non-applanating interface design Must allow for personalization of surgical procedures Must be capable of providing a stable Intraocular pressure Must minimize the occurrence of corneal folds Must be sterile Must be for single patient utilization Must be capable of centering and fixating the patients eye to the system Utilize an annular ring or equivalent mechanism to apply suction to the patients eye 12mm Daily Verification Tools - 1 each EQUIVALENT TO: Abbott Medical Optics/ SA-08044 Specifications/Salient Characteristics: This is a disposable item that is utilized to perform daily verification of the Cataract Femtolaser System Must be compatible with Cataract Femtolaser System Daily Alignment Verification Interface - 10 each EQUIVALENT TO: Abbott Medical Optics/ SA-09522 Specifications/Salient Characteristics: This is a disposable item that is utilized to perform daily alignment verifications of the interface aspect of the Cataract Femtolaser System Must be compatible with Cataract Femtolaser System Catalys Extended Warranty - One (1) Year Catalys Essential Characteristics Essential Characteristics (1) femtosecond pulse laser for cataract surgery [28-161]. The system shall be a diode-pumped solid state ophthalmic laser with a wavelength in the near-infrared spectrum designed for use in cataract surgery. The system shall be FDA-approved for anterior capsulotomy, single- and multi-plane corneal cuts/incisions, and phacofragmentation for nuclear, subcapsular, and cortical cataracts. The system shall be indicated for use in patients diagnosed with glaucoma. The system shall be capable of performing each of these operations individually and consecutively. The system shall feature pulse durations in the femtosecond range (<600 femtoseconds) and pulse frequencies greater than 100 Hz. The system shall be capable of conducting three-dimensional Fourier-domain (spectral-domain) optical coherence tomography (OCT) for visualization during the operation. The system shall feature a nonapplanating liquid patient interface (docking system) with intraocular pressure increases no greater than 15 mmHg. The system shall feature automated tilt correction. The system shall include a safety feature to prevent veering from the desired operating area. The system shall include an integrated patient bed. The system shall run an approved operating system and include all hardware and software necessary for full system functionality. Electrical requirements are 220 VAC, 60 Hz. Vendor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor or authorized reseller for the proposed equipment/system, such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions. The systems 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.
 

Web Link

FBO.gov Permalink
(https://www.fbo.gov/spg/VA/AlVAMC502/AlVAMC502/36C25618Q9448/listing.html)
 

Document(s)

Attachment
 

File Name: 36C25618Q9448 36C25618Q9448.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=4331746&FileName=36C25618Q9448-000.docx)

Link: https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=4331746&FileName=36C25618Q9448-000.docx

 

Note: If links are broken, refer to Point of Contact above or contact the FBO Help Desk at 877-472-3779.
 

Record

SN04934116-W 20180526/180524230706-4688f5c2bf8923cc97098dd993a55a76 (fbodaily.com)
 

Source

FedBizOpps Link to This Notice
(may not be valid after Archive Date)

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