MODIFICATION
65 -- COST PER TEST REAGENTS AND ANALYZERS
- Notice Date
- 9/15/2014
- Notice Type
- Modification/Amendment
- NAICS
- 334516
— Analytical Laboratory Instrument Manufacturing
- Contracting Office
- Department of the Army, U.S. Army Medical Command, Southeast Regional Contracting Office, ATTN: MCAA SE BLDG 39706, 39706 40th Street, Fort Gordon, Georgia, 30905-5650
- ZIP Code
- 30905-5650
- Solicitation Number
- W81K0014R4424
- Archive Date
- 10/8/2014
- Point of Contact
- Valerie DeVeaux, Phone: 7067878438
- E-Mail Address
-
valerie.j.deveaux.civ@mail.mil
(valerie.j.deveaux.civ@mail.mil)
- Small Business Set-Aside
- N/A
- Description
- The purpose of this modification is to revise the salient characteristics. Chemistry Features/Benefits The System Must: •Have no plumbing, drains, stirring mechanisms, mixing assemblies floor vents, or deionized water. •Have no stand-by mode system, be always available/in normal operation. •Be ergonomically designed with flat touch screen monitor. •Have on-board documentation and help functions. •Have system waste contained within the system and disposed of daily. •Not allow sample and or reagent carryover. •Not have dedicated reagent positions. •Require minimal reagent preparation. •Have liquid reagents which must be capped while onboard. •Run multiple user defined assays at one time. •Have flexible processing for routine and STAT testing. •Have positive patient identification via on-board barcode scanner. •Throughput of up to 300 results per hour. •Have on-board dilution. Specifically, auto dilution, auto repeat and auto reflex capability. •Be self-monitoring and alert operators to prompt action, avoiding testing delays. •Provide sample management with clot detection, bubble detection, liquid level-sensing, short-sample detection. The system must save the sample if a clot or bubble is detected during primary aspiration. •Be able to determine hemolysis, icterus and turbidity levels without additional patient sample, reagents, consumables and no effect on throughput. It must flag only assays affected by the interferent. It must send flags and level to the LIS or data management system. •Therapeutic monitoring drugs (TDM) must be available on system. •Must use assays that are in a dry thin film layered format for general chemistry profiles. •Have HDL, LDL, HBA1C assays which require no pretreatment. •Support multiple lots onboard and automatically switch lots when one is depleted. •Offer extended calibration stability with the same lot. •Only calibrate assays at lot change, when critical system parts are changed due to service or maintenance, if QC results are consistently outside acceptable ranges, or when government regulations require, i.e., 6 months in US. •Provide host query and broadcast download capability •Use disposable wells provided by the manufacture for samples which prevent sample carryover and decrease error. •Be able to utilize: chemiluminescence technology •Have at least on-board test capacity of 2000 tests. •All assays can be programmed and calibrated at once. •Utilize Sample Volume: 10-80 µL •Have all components necessary to process an assay in a ready-to-use, single universal package. •Troponin assay that offers superior sensitivity and demonstrates excellent distinction between normal ranges of plasma troponin levels and clinically significant levels of plasma troponin.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/USA/MEDCOM/DADA08/W81K0014R4424/listing.html)
- Place of Performance
- Address: Winn Army Community Hospital, 1061 Harmon Ave, Fort Stewart, Georgia, 31314, United States
- Zip Code: 31314
- Zip Code: 31314
- Record
- SN03511672-W 20140917/140915235931-d9aba8be2e218ee73fcec32d771b6f73 (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
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