ATTACHMENT A - SALIENT CHARACTERISTICS - IMMUNOLOGY TESTING SUPPLIES.docx

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Attached to
6550--IMMUNOLOGY TESTING SUPPLIES Federal contract opportunity
Solicitation number
36C26225Q0194
Issued by
Department of Veterans Affairs Veterans Health Administration Veterans Integrated Service Network 22

About this file

This is a salient characteristics document detailing requirements for immunology testing supplies for the VA Southern Arizona Healthcare System in Tucson. The document specifies Bio-Rad brand name or equal products including D-100 CPR Billing supplies, analytical cartridges, calibrator packs, buffers, wash solutions, and microvials, with specific product numbers and quantities listed.

The supplies must be FDA-approved and compatible with Bio-Rad's BioPlex 2200 analyzer and Unity Real Time software. The vendor must provide monthly evaluations including laboratory performance reports, secure continuity between reagent lots, distribute products within 2 days of order, and send monthly reserve reports of sequestered quality control. The solicitation (36C26225Q0194) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) set-aside with responses due December 11, 2024, at 4:00 PM PT. Questions are due by December 6, 2024. The period of performance is one base year with delivery to the VA facility in Tucson, AZ.

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ATTACHMENT B - SCHEDULE OF PRICING - IMMUNOLOGY TESTING SUPPLIES.xlsx XLSX spreadsheet
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Text version

VA Southern Arizona (Tucson) Healthcare System Immunology Testing Supplies

1. BRAND NAME OR EQUAL

BRAND
PRODUCT DESCRIPTION
PRODUCT #
QTY
Bio-Rad
D-100 CPR Billing

19000041

54000

Bio-Rad
Analytical Cartridge/Calibrator Pack
2901004
1
Bio-Rad
Prefilter (5 per package)
2901007
1
Bio-Rad
Elution Buffer A
2901010
9
Bio-Rad
Elution Buffer B
2901011
3
Bio-Rad
Wash Solution
2901012
9
Bio-Rad
Sample Diluent
2901009
3
Bio-Rad
D-100 Microvials (100 per package)
12000243
3
Bio-Rad
Calibrator Pack
2901006
1
Bio-Rad
Cleaning Tube
2901008
1

2. SALIENT CHARACTERISTICS

Obtain chemistry immunology reagents and consumables, these supplies must have the following characteristics:

1. The reagents, consumables and supplies must be approved for use with Bio-Rad’s, BioPlex 2200.

2. All supplies, reagents, controls, calibration materials, disposables, and any consumable parts necessary for analyzer operation, must be Food and Drug Administration (FDA) approved.

3. The quality control results generated from all tests performed with BioPlex 2200 must be compatible with Unity Real Time software.

3. STATEMENT OF WORK

1. The vendor must generate and provide monthly evaluations with the following reports:

a. Laboratory Performance Overview

b. Laboratory Comparison Report

c. Laboratory Histogram

2. To secure continuity between lots of reagents and consumables the vendor should be able to directly sequester reagents and consumables from the lots currently being used.

3. The vendor must directly distribute all requested products no more than 2 days after receipt or order (ARO).

4. The vendor must send monthly updated reserve reports of sequestered quality control.

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