Inactive

This solicitation is for Sperm Quality Analyzer (SQA) for the Landstuhl Regional Medical Center in Germany. The contract type will be a Firm-Fixed-Price (FFP) Purchase Order as a result of the solicit... This solicitation is for Sperm Quality Analyzer (SQA) for the Landstuhl Regional Medical Center in Germany. The contract type will be a Firm-Fixed-Price (FFP) Purchase Order as a result of the solicitation. It is incumbent upon interested parties to review this site frequently for any updates/amendments to any and all documents. Purchase Order will be issued using Lowest Price Technically Acceptable (LPTA) evaluation techniques. All vendors must be registered in the System for Award Management (SAM) prior to award, and lack of registration shall make a quotation ineligible for award. Vendors may obtain information on registration and annual confirmation requirements by calling 1-866-606-8220 or via Internet at https://www.sam.gov. Technical Factor. The quoter must demonstrate compliance with the requirements in the solicitation by submitting a written quote which addresses compliance with each of the following technical factors: Subfactor 1: The delivered equipment shall be new and not a used or re-manufactured product. Subfactor 2: Equipment must have a minimum warranty of 12 months. Subfactor 3: Equipment must comply with German electrical requirements of 220V/50Hz and have a European two-prong power plug. Subfactor 4: Equipment must be capable to perform automated semen analysis, including motility, progressive and non-progressive motility, immotility, morphology, and counts in accordance WHO standards, 5th addition. Subfactor 5: Equipment must be capable to analyze fresh specimens and post-vasectomy specimens in less than five minutes. Subfactor 6: Equipment must be capable to interface with laboratory’s information system, Composite Health Care System (CHCS). Subfactor 7: Equipment must include all peripheral equipment (monitor, printer, etc.) required for operation. Subfactor 8: Quote must include validation kit for the initial validation of accuracy, precision, and reportable range in accordance with Clinical Laboratory Improvement Amendments (CLIA). Subfactor 9: Must possess FDA certification with no greater than moderate complexity under CLIA. Subfactor 10: Quote must include software, operator manual, service manual and all relevant safety data sheets in English language. Subfactor 11: Quote must include on-site installation and training for three (3) users. Failure to receive an Acceptable rating of any of the above technical evaluation factors / salient characteristics will result in an Unacceptable technical rating unless the error(s), deficiency (ies) or omission (s) can be corrected. *************************************************************************** * See Addendum to 52.212-1 for Instructions to Offerors. * *************************************************************************** * Ensure to complete provisions 52.204-24, 52.204-26, 52.209-2 & 52.209-11 * ***************************************************************************