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This Government Contract opportunity from Department Of Defense was posted on September 28, 2016. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Blood Grouping

Awarded
N6809516RC05052Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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NAICS: 325413
New
DIBBS
CULTURE MEDIUM, THAYER-
Solicitation # SPE2DS-27-T-1066
Solicitation SPE2DS-27-T-1066 is a request for quotations issued by the DLA Troop Support Medical Supply Chain for the procurement of one package of Thayer-Martin Modified (MTM II) Agar culture medium, identified by NSN 6550-01-711-1542. This dark brown, ready-to-use plated medium is specifically designed for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. The product is delivered in packages of 100 plates and requires strict refrigeration storage between 2 to 8 degrees Celsius (36 to 46 degrees Fahrenheit) and must not be frozen. The contract mandates a non-extendable shelf life of three months, with a requirement that no more than 14 days elapse between the date of manufacture and the date of delivery to the government. Delivery is set for JBER, Alaska, with a required delivery date of October 27, 2026, under FOB Destination terms. Packaging must be commercial and sealed to prevent damage, with marking adhering to Medical Marking Standard No. 1 and shelf-life labels following MMS1C. Administrative requirements include electronic invoicing via the Wide Area WorkFlow system and compliance with various FAR and DFARS clauses, including the Buy American Act, Berry Amendment, and safeguarding of covered defense information. Evaluation will consider technical data for any alternate products offered and may include HUBZone price evaluation preferences. Inspection and acceptance will occur at the destination.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

1 day ago

DEADLINE

in 4 days
NAICS: 325413
New
Federal
6550--Optilite analyzer reagents
Solicitation # 36C26227Q0052
The Department of Veterans Affairs, Southern Arizona Healthcare System, is soliciting a Firm-Fixed Price Blanket Purchase Agreement under solicitation 36C26227Q0052 for the procurement of FDA-approved reference testing reagents and consumables validated for use on the Optilite analyzer. The scope includes specific items such as Freelite Kappa, Freelite Lambda, and Ceruloplasmin reagents, as well as TENCELL cuvettes and sample cups. To ensure system performance and safety, all materials must be manufactured by Binding Site Laboratories, and substitutions are prohibited. The contract is issued as a full and open competition under NAICS code 325413, with a total estimated period of performance of sixty months, consisting of a base period from November 9, 2026, to November 8, 2027, followed by four one-year option periods. The award will be granted to the responsible offeror whose proposal is most advantageous to the government, based on a technical acceptability review of the Statement of Work and the lowest price. Deliveries are required to be made to various VA Medical Centers across Arizona, California, and New Mexico, with standard orders delivered within four working days of placement. All shipments must be destination-based, with the vendor assuming all shipping costs and adhering to strict packaging standards to prevent damage. Invoicing is handled electronically through the Department of Veterans Affairs Financial Services Center in accordance with the Prompt Payment Act. Quotes must be submitted via email to Contract Specialist Carlos Magana by November 4, 2026.
262-NETWORK Contract Office 22 (36C262)

POSTED

3 days ago

DEADLINE

in 5 days
NAICS: 325413
New
Federal
BPA - Consumable Supplies for Terumo Trima Accel Blood Collection systems
Solicitation # HT942627QE003
The Defense Health Agency is soliciting quotations to establish a Blanket Purchase Agreement (BPA) for the recurring resupply of consumable products for three Terumo Trima Accel Blood Collection Systems used by the USAISR Combat Casualty Care Research Team 1 in Texas. To maintain FDA approval and satisfy research protocols, the contractor must provide original manufacturer-supplied consumables, including Teruflex 500ml collection bags, Trima Platelet Kits, Isoplate Solution (PAS-F), TSCD Wafers, ACD-A Solution, and 150 mL couplers. This procurement is a 100 percent set-aside for Service-Disabled Veteran-Owned Small Businesses under NAICS 325413. The resulting BPA will have a 60-month ordering period with a total ceiling of 35 million dollars, though some documentation notes a lower limit of 350,000 dollars. Individual call orders are capped at 50,000 dollars, while Government Purchase Card orders are limited to 15,000 dollars. Awards will be made on a Lowest Price Technically Acceptable basis, with technical capability rated as pass or fail. All payment requests and receiving reports must be processed electronically through the Wide Area WorkFlow system. Quotations are due by November 6, 2026, and must be submitted in two separate volumes covering technical capability and pricing.
Army Medical Resources Acq Activity

POSTED

7 days ago

DEADLINE

in 7 days
NAICS: 325413
Federal
6550--VISN Cepheid GeneXpert Testing Supplies Base Plus 3 Op Yr RFQ
Solicitation # 36C24527Q0042
The Department of Veterans Affairs, specifically the VA North Atlantic Health Network (HSA 1.3), is soliciting a firm-fixed-price, Indefinite Delivery/Indefinite Quantity (IDIQ) contract for Cepheid GeneXpert testing supplies. This requirement covers the procurement of FDA-approved reagents, consumables, and service for PCR analyzers to detect various pathogens, including CoV-2, Influenza, RSV, MRSA, and Mycobacterium Tuberculosis. The contract is structured with a base period ending October 31, 2027, and three subsequent one-year option periods extending through October 31, 2030. Deliveries will be made to multiple VA Medical Centers across Maryland, West Virginia, and Washington DC. This acquisition is set aside for HUBZone small businesses. Award will be determined using the Lowest Price Technically Acceptable (LPTA) method, evaluating technical acceptability, delivery performance, past performance, and price, with additional credit given to certified SDVOSB or VOSB offerors. Key contractor requirements include being an authorized distributor, acknowledging orders within 24 hours, and guaranteeing a minimum four-month expiration date on reagents. Additionally, the vendor must provide an emergency plan to deliver replacement supplies within 24 hours if products are found to be defective. Invoices must be submitted electronically, and payments will be processed in accordance with the Prompt Payment Act.
245-NETWORK Contract Office 5 (36C245)

POSTED

8 days ago

DEADLINE

in 6 days

AI Contract Overview

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The Naval Medical Logistics Command intends to negotiate a sole source contract with Ortho Clinical Diagnostics to provide two automated hematology blood grouping analyzers for Naval Hospital Bremerton and Naval Hospital Oak Harbor. The requirement includes the equipment, consumable supplies, and comprehensive maintenance support. These systems must utilize gel technology to perform a wide range of tests, including ABO/Rh grouping, antibody screens, and crossmatching, while supporting annual workloads of 9,200 and 5,000 specimens respectively. The analyzers must be fully automated, FDA compliant, and capable of handling various sample types with barcode tracking and STAT access. The contract encompasses installation, validation, onsite and offsite training, and preventive maintenance. The period of performance consists of a one-year base term with four optional one-year extensions. The contractor is required to be an authorized OEM dealer or distributor to ensure all warranties and services are maintained. This acquisition is conducted under simplified acquisition procedures and is classified under NAICS code 325413. The vendor is responsible for the delivery, uncrating, and installation of the benchtop units in compliance with OSHA requirements.

General Info

Contract Value

$0

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

MD, USA

Set-Aside

NONE

Award Issued Date

Documents

1

Attachment_VI-JA-N6609716RC05027-N6809516RC05052-Base-CPRR_Oak_HarborBremerton_Redacted.pdf

PDF

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Timeline

1 update
PhaseAwarded
Posted

Presolicitation

Notice updated

Notice type changed from Presolicitation to Solicitation. The notice description changed.

Awarded

Contract was awarded

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → Naval Medical Logistics Command
Contacts1 person available
OfficeFORT DETRICK, MD, 21702-9203, USA
Office AddressFORT DETRICK, MD, 21702-9203, USA

Full Description

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The Naval Medical Logistics Command intends to negotiate on a sole source basis (IAW FAR 13.501) with Ortho Clinical Diagnostics, 1001 US Highway 202, Raritan, NJ 08869. The requirement is for a contract which includes equipment, maintenance support, and consumable supplies for one (1) Analyzer, Laboratory, Hematology, Blood Grouping, Automated [16-817] for Naval Hospital Bremerton and one (1) Analyzer, Laboratory, Hematology, Blood Grouping, Automated [16-817] for Naval Hospital Oak Harbor. The system shall be capable of performing at least the tests listed below for a minimum annual workload of 9,200 specimens for Naval Hospital Bremerton and 5,000 specimens for Naval Hospital Oak Harbor. TEST ABO/Rh Grouping ABO/Rh Confirmation Antibody Screens Antibody Identification Selected Cell Panel Rh Phenotype (C,c,E,c) Donor Confirmation Crossmatch (AHG) Antigen Typing Serial Dilutions for Titration Studies DAT (Polyspecific) DAT (IGG) Cord Blood Testing The system shall be capable of performing blood bank testing using gel technology. The system shall be fully automated and provide functions including liquid pipetting, serial dilution, reagent handling, incubation, reaction grading, reaction interpretation, and data management. The system shall provide critical process monitoring and allow for management of system maintenance and quality control. The system shall be capable of using the following sample types: centrifuged whole blood, plasma, serum, and packed red blood cells. The system shall be capable of barcode tracking. The system shall be capable of identifying reagents and specimens. The system shall be capable of continuous, random, STAT access, and batch specimen processing modes. The system shall accommodate batch processing interruptions to insert STAT specimens into the workflow. The system shall be capable of holding test tubes of various sizes. The system shall include a manual backup workstation. The system shall be benchtop with maximum physical dimensions of 36" tall, 42" wide, 32" deep, and shall weigh at most 450 lbs. The electrical requirements are 100VAC, 60 Hz. System installation, validation, correlation, onsite and offsite training, and preventive maintenance coverage shall be included. Yearly off-site training for key operator staff shall be provided. On-site assistance during validation shall be provided. Corrective system maintenance coverage shall include response times as specified in the Statement of Work. Support shall be provided for a period of performance for one year with option years available for four (4) consecutive year terms after the base year term. The units shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. The system shall be installed in compliance with OSHA requirements. Contractor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor or authorized reseller for the proposed equipment/system such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions. Upon delivery, the contractor shall be responsible for uncrating the unit/system, transporting it through the facility to the location of intended use for installation, and removing of all trash created in this process. If interim storage is required, the vendor shall make arrangements for the storage. This acquisition is being conducted under simplified acquisition procedures FAR 13.501 under the authority of the test program for commercial items (section 4202 of the Clinger-Cohen Act of 1996). There are not set-aside restrictions for this requirement. The intended procurement will be classified under North America Industry Classification System (NAICS) 325413 with a small business size standard of 1250. This notice of intent is not a request for competitive proposals and no solicitation document exists for this requirement. However, parties interested in responding to this notice will need to submit technical data sufficient to determine capability in providing the same product. All capability statements received by the closing date of this synopsis will be considered by the Government. A determination by the Government not to compete based on responses to this notice is solely within the discretion of the Government. Information received will be considered solely for the purpose of determining whether to conduct a competitive procurement. Capability statements shall be submitted by email only as a MS Word or Adobe PDF attachment to Derek Bell at contact@example.gov. Statements are due not later than 11:00 AM EST on 12 Aug 16. No phone calls accepted.

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