Public Display Solicitation
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Q15001308 Rapid HIV Antigen/Antibody Test Kits and Controls
- Solicitation Number
- Q15001308
- Status
- Awarded
- Department
- Health
- Division
- Communicable Disease Division
- Islands (where the work/delivery is to be performed)
- Statewide
- Category
- Goods and Services
- Release Date
- 05/07/2015
- Offer Due Date & Time
- 05/15/2015 02:00 PM
- Description
- Rapid HIV Antigen/Antibody Test Kits and Controls
- Contact Person
- Shigemura, Millie
- mildred.shigemura@doh.hawaii.gov
- Phone
- 808-733-9281
- General Comments
- VENDOR MUST BE REGISTERED AND COMPLIANT IN HAWAII COMPLIANCE EXPRESS (HCE).
BID PRICES MUST BE DELIVERED PRICES TO INCLUDE ALL TRANSPORTATION, TAX, SHIPPING, HANDLING CHARGES, AND IN PERSON TRAINING. THE VENDOR WILL BE RESPONSIBLE FOR DELIVERY TO THE POINTS OF DESTINATION.
RAPID HIV ANTIGEN/ANTIBODY TEST KITS AND CONTROLS SHOULD HAVE THE LONGEST EXPIRATION DATE POSSIBLE.
DELIVERY DATE: June 15, 2015
IN PERSON PRODUCT TRAINING WILL BE NEEDED ON 4 ISLAND COUNTIES.
Please contact Michelle Wozniak for more information regarding this solicitation. Her email address is Michelle.Wozniak@doh.hawaii.gov and phone number is (808) 733-4387. - Procurement Officer
- Phillip Nguyen
- Attachments
-
Delivery Instructions 2015.pdf
Download All
Direct all questions regarding this Solicitation, and any questions or Issues relating to the accessibility of this Solicitation (Including the appendices and exhibits to this Document, and any other document related to this Solicitation), to: Shigemura, Millie.
Q15001308 Rapid HIV Antigen/Antibody Test Kits and Controls
#
Title
Quantity
Unit of Measure
Commodity Code
Commodity Code | Description |
---|---|
19389 | Test Kits and Supplies, Chemistry (Not Otherwise Classified) |
- Quantity
- 9500
- Unit of Measure
- EACH
- Title
- Rapid HIV Antigen/Antibody Test Kits
- Description
- Rapid HIV Antigen/Antibody Test Kits
- The test kit must detect both HIV 1/2 antibodies and HIV 1 P24 antigens.
- The test kit must be CLIA waived and FDA approved for use with fingerstick whole blood and veni-puncture whole blood specimens.
- The test kit must be spill resistant if knocked over.
- The test kit shelf-life must be at least 12 months.
- The rapid HIV Antigen/Antibody controls must be compatible with the rapid HIV test kit to ensure its proper performance.
- In person product training to 4 island counties.
Commodity Code | Description |
---|---|
19389 | Test Kits and Supplies, Chemistry (Not Otherwise Classified) |
- Quantity
- 100
- Unit of Measure
- EACH
- Title
- Rapid HIV Antigen/Antibody Controls
- Description
- Rapid HIV Antigen/Antibody Controls
- The test kit must detect both HIV 1/2 antibodies and HIV 1 P24 antigens.
- The test kit must be CLIA waived and FDA approved for use with fingerstick whole blood and veni-puncture whole blood specimens.
- The test kit must be spill resistant if knocked over.
- The test kit shelf-life must be at least 12 months.
- The rapid HIV Antigen/Antibody controls must be compatible with the rapid HIV test kit to ensure its proper performance.
- In person product training to 4 island counties.
Direct all questions regarding this Solicitation, and any questions or Issues relating to the accessibility of this Solicitation (Including the appendices and exhibits to this Document, and any other document related to this Solicitation), to: Shigemura, Millie.