Urinalysis Analyzer Salient Characterisitics.docx
DOCX document 14 KB Posted
- Attached to
- Urinalysis Reagents & Analyzer System Federal contract opportunity
- Solicitation number
- PANHCA-21-P-004954
- Issued by
- Department of the Army Medical Command
About this file
This sources sought notice requests capability statements from interested businesses to provide a fully automated urinalysis analyzer system, inclusive of instruments, ancillary equipment, reagents, quality control materials, calibrators, tubes, racks and additional items to complete testing at Madigan Army Medical Center. Interested parties should submit capability statements no more than ten pages demonstrating their ability to provide the required products and services, as well as service, maintenance, training, repairs and support to keep the urinalysis analyzer system performing in optimal conditions. Capability statements must be submitted electronically to the Contract Specialist by 12:00 p.m. Pacific Time on April 15, 2021, referencing the synopsis number. The period of performance is expected to be from October 1, 2021 through September 30, 2026, with the base period plus four optional one-year extensions. The applicable NAICS code is 325413 and size standard is 1,250 employees.
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| File | Type | Posted |
|---|---|---|
| Urinalysis Analyzer SOW.docx | DOCX document |
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Text version
Urinalysis Salient Characteristics The Contractor shall provide Urinalysis Reagents used in support of the urinalysis mission at Madigan Army Medical Center, Joint Base Lewis McChord, WA. The Contractor shall be responsible for furnishing a fully automated Urinalysis analyzer system (inclusive of instruments, ancillary equipment (computer, external drives, printer, UPS, sturdy wheeled table, etc.), maintenance, services, repairs, support, and parts as required in order to maintain the systems in optimal operating condition at no extra cost to the Government.
1. Must be able to integrate and scale-up on a single automated line to meet future testing/ workflow needs. (3.2.1)
2. Must include the flexibility to allow operator to use a STAT port of entry at the individual modules or a single routine point of entry to analyze all of the required tests. (3.2.1.1)
3. Must provide true walkaway final results without operator re-classification of urine particles to standardize interpretation and remove operator subjectivity. (3.2.1.2)
4. Must have auto-validation capability for RBCs, WBCs, Casts, Bacteria, and Epithelial Cells reducing time used for tech review and manual release. (3.2.2).
5. Must include a urine digital imaging analyzer with microscope quality images. (3.2.2)
6. Must offer a floor standing model with scalable automation line configurations. (3.1.1.1)
7. Must offer reagent storage wagons/ tables/ carts. (3.1.1.1)
8. Must be able to remove common interferences through a warming function, reagents that dissipates amorphous urate and phosphate material or other technology. (3.2.2)
9. Must provide a urine chemistry analyzer that can perform automatic color correction to compensate for darkly colored urines and correct result for applicable parameters. (3.2.2)
10. Must be able to interface with Data Innovations Instrument Manager (IM). (3.6.1)
11. All instruments must be connect through one control unit. (3.2.2)
12. There must be one TCP/IP connection to IM. (3.2.2)
13. The entire process must be fully automated. (3.1.1)
14. The system must provide redundancy to maintain 24/7 operations.(3.1.1)
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