ATTACHMENT A - SALIENT CHARACTERISTICS - IMMUNOLOGY TESTING SUPPLIES.docx

DOCX document 20 KB Posted

Attached to
6550--IMMUNOLOGY TESTING SUPPLIES Federal contract opportunity
Solicitation number
36C26224Q0234
Issued by
Department of Veterans Affairs Veterans Health Administration Veterans Integrated Service Network 22

About this file

This document outlines the salient characteristics for immunology testing supplies required by the VA Southern Arizona Healthcare System. The supplies must be approved for use with Bio-Rad's BioPlex 2200 and D-100 instruments and include reagents, consumables, controls, calibration materials, and disposables necessary for analyzer operation. All items must be FDA approved. The quality control results generated from BioPlex 2200 testing must be compatible with Unity Real Time software. The vendor must also provide monthly evaluation reports covering laboratory performance, comparisons, and histograms. To ensure continuity, the vendor should be able to directly source currently used reagent and consumable lots. All ordered products must be distributed no more than two days after receipt of order to avoid testing delays.

The related federal contract opportunity is solicitation number 36C26224Q0234 for immunology testing supplies issued by the Department of Veterans Affairs VHA VISN 22. The supplies outlined in the salient characteristics document are the subject of this solicitation.

View the file

Other files for this federal contract opportunity

Other files attached to 6550--IMMUNOLOGY TESTING SUPPLIES, newest first.
File Type Posted
ATTACHMENT B - SCHEDULE OF PRICING - IMMUNOLOGY TESTING SUPPLIES.xlsx XLSX spreadsheet
36C26224Q0234.docx DOCX document

On GovTribe

Work with this file on GovTribe

  • Download the original file
  • Contacts named in this file
  • Similar government files
  • Ask GovTribe AI about this file

Text version

VA Southern Arizona (Tucson) Healthcare System Immunology Testing Supplies

1. BRAND NAME OR EQUAL

BRAND
PRODUCT DESCRIPTION
PRODUCT #
QTY

Bio-Rad

HIV Ag-Ab Manual Reagent Pack Piercer
6600306
2
Bio-Rad
BPX Sodium Hydroxide 1N
6600578
1
Bio-Rad
BPX, Rack, Sample:x30
6600800
1
Bio-Rad
BPX Syringe w/Teflon Seal 2.5mL RoHS
6600809
1
Bio-Rad
BPX 2200 Sheath Fluid, 2 PA
6600817
24
Bio-Rad
BPX2200 Wash Buffer
6600818
40
Bio-Rad
BPX Bag Waste Biohazard 14x19
6600820
10
Bio-Rad
BPX Vessel Reaction 1000/bag
6602003
30
Bio-Rad
BPX Detector Calibration Pack
6660001
12
Bio-Rad
BPX Detector Clean Pack
6660002
12
Bio-Rad
BPX Probe Cleaning Sol. Btls (4)
6660003
12
Bio-Rad
Cap, Screw 2mL Neutral 500/bag
25222B
6
Bio-Rad
BP22 Probe Reagent Sample SS RoHS
12000449
1
Bio-Rad
ANA Screen Calibrator Set
6631101
12
Bio-Rad
CD BPX Cal. Value AssignmentANA
6631121
6
Bio-Rad
BPX Control Set, ANA Screen
6631131
12
Bio-Rad
CD BPX CtrlValue AssignmentANA
6631141
6
Bio-Rad
BPX ANA Screen, 100 tests
6651150
40
Bio-Rad
Cal Set, Celiac IgA, BPX
6632300
12
Bio-Rad
CD, Cal Val Asgn, Celiac IgA, BPX
6632320
6
Bio-Rad
Ctrl Set, Celiac IgA, BPX
6632330
12
Bio-Rad
CD, Ctrl Val Asgn, Celiac IgA, BP
6632340
6
Bio-Rad
Celiac IgA, 100 test, BPX
6652350
12
Bio-Rad
BPX Calibrator Set, Anti-CCP
6633200
12
Bio-Rad
CD, BPX Calibrator, Anti-CCP
6633220
6
Bio-Rad
BPX Control Set, Anti-CCP
6633230
12
Bio-Rad
CD, BPX Control Valve, Anti-CCP
6633240
6
Bio-Rad
BPX Anti-CCP IgG, 100 tests
6653250
18
Bio-Rad
D-100 CPR Billing

19000041

54000

Bio-Rad
D-100 HBA1C Calibrator Pack (CPT)
2901006
TBD
Bio-Rad
Cap, Screw 2ml Neutral 500/bag (CPT)
25222B
TBD
Bio-Rad
D-100 HBA1C Cart & Cal Pack (CPT)
2901004
TBD
Bio-Rad
D-100 HBA1C Prefilter Set (CPT)
2901007
TBD
Bio-Rad
D-100 System Cleaning Tube (CPT)
2901008
TBD
Bio-Rad
D-100 Sample Diluent (CPT)
2901009
TBD
Bio-Rad
D-100 Buffer A (CPT)
2901010
TBD
Bio-Rad
D-100 Buffer B (CPT)
2901011
TBD
Bio-Rad
D-100 Wash Solution (CPT)
2901012
TBD

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 and D-100.

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.

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

a. Laboratory Performance Overview

b. Laboratory Comparison Report

c. Laboratory Histogram

5. 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.

6. To avoid delays in patient testing the vendor must take orders and directly distribute all requested products no more than 2 days after receipt or order (ARO).

File details come from the government source that posted it. Updated .