The RFP Database
New business relationships start here

Advia 120 Reagents


Maryland, United States
Government : Federal
RFP
Go to the link
This document has expired, therefore the above link may no longer work.

THIS IS NOT A REQUEST FOR PROPOSALS (RFP) OR A REQUEST FOR QUOTATIONS (RFQ); NO CONTRACT WILL BE AWARDED PURSUANT TO THIS ANNOUNCEMENT.
This synopsis is for information and planning purposes only and is not to be construed as a commitment by the government. This is NOT a Request for Proposal, Invitation for Bid, or an announcement of a solicitation. Response to this SOURCES SOUGHT is strictly voluntary and will not affect any firms' ability to submit an offer if a solicitation is released. There is no bid package or solicitation document associated with this announcement. The purpose of this document is to identify potential sources. Any requests for a solicitation package will be disregarded. The Government does not intend to award a contract on the basis of this source sought or otherwise pay for the information solicited. No entitlement to payment of direct or indirect costs or charges by the Government will arise as a result of preparing submissions in response to this sources sought and the Government's use of such information.
This sources sought is being conducted to identify potential Small Manufactures/Authorized Distributors capable of producing or supplying Brand Name Supplies.
SCOPE OF WORK

Catalog Number Description Quantity
T01-3621-52 ADVIA DIFF Timepac 20 each
T01-3620-52 ADVIA CBC Timepac 20 each
T03-3682-54 OptiPOINT Calibrator 4 each
T03-3685-52 SETpoint Calibrator 4 each
T03-3688-54 TESTpoint Control - High 9 each
T03-3686-54 TESTpoint Control - Low 9 each
T03-3687-54 TESTpoint Control - Normal 9 each
T01-3625-54 ADVIA Defoamer 6 each
4871500 ADVIA EZ WASH 40 each
113-3719-01 Filter, Clot 40 each
T01-3633-54 Perox Sheath 20 each
518-7074-01 Filters, Drain 6 each
065-B075-01 Lamp Assy. Perox 2 each
Period of Performance:
The period of performance for these products is one (1) year. July 1, 2017 - June 30, 2018.


Delivery Schedule:
The Cell Processing Section has delivered a standing order schedule to the company. The company shall comply by sending the materials per the standing order schedule.


Scope of Work:
The Contractor will supply sufficient reagents and disposables to process numerous assay samples per year.
Shelf Life-Minimum - shelf life of any unopened reagent shall be at least 60 days unless otherwise agreed to from date of delivery at the DTM Cell Processing Laboratory. Shelf Life of disposables shall be at least 3 months from date of delivery at the DTM Cell Processing Laboratory.
The reagents and disposables may include but not limited to those listed above.


Objective:
Advia reagent kits and accessories are needed to perform advanced cell counts and must be used in conjunction with the ADVIA System purchased in 2015. Regarding the system/instrument, it provides a superior system for analyzing samples that do not contain hemoglobin (i.e., samples of cells in clear solutions). The Advia analyzer has broader linearity for detection of low red and white blood cell counts, high white blood cell and platelet counts which are needed for cell counting of FDA licensed red blood cell and platelet concentrates and cellular therapy products manufactured under FDA investigational new product applications.


 


 



The proposed vendor, Siemens, is the only known vendor that manufactures the Siemens kits and accessories for the Siemens Advia instrumentation purchased in 2015 due to the current analyzer in use, Abbott Cell-Dyn 3700, being phased out by the company. This Siemens was the only comparable clinical analyzer with the capability of performing cells counts using a veterinary program. These kits and accessories permit the analysis of cells that undergo expansion in X Vivo cell culture. This allows for not only cell counts but also the specific type of cells. These kits (and accessories) via the Advia analyzer allow for the detection of low red and white blood cell counts, high white blood cell and platelet counts which are needed for cell counting of FDA licensed red blood cell and platelet concentrates an cellular therapy products manufactured under FDA investigational new product applications. If we were not able to procure this, the protocols would have to be discontinued as the Cell Processing Section would not be able to manufacture blood products required for patient care. This could be fatal.


CAPABILITY STATEMENT - Any potential Manufacturer must demonstrate the following:
1) The offeror shall submit product literature for the supplies it is proposing. Capability Statement(s) should clearly identify the following:
a. Name of the Manufacturer, quantity and location where the units are produced (domestic and/or international);
b. A signed statement to state, "We are the Manufacturer of the items and/or we are authorized distributors of company X";
c. Estimated Number of days, after receipt of order that is typical for delivery of such items;
d. Any other relevant information that is not listed above which the Government should consider in developing its minimum specifications and finalizing its market research.


2) Provide the following business information:
a. DUNS number
b. Company Name
c. Company Address (including point of contact, phone number and email address)
d. Type/Size of company, NAICS code as validated in SAMS.
Respondents will NOT be notified of the results of the evaluation.


Andre M. Moody, Contract Specialist , Phone 3014022677, Fax 3015945925, Email moodya@cc.nih.gov

    1. Home
    2. Articles
    3. Login or Register

    4. Search

    5. Add/Announce your RFP