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MICROGENICS CORPORATION Fremont CA USA

UEI: SLED_BA222F988CE579E3

MICROGENICS CORPORATION Fremont CA USA is a federal contractor, registered under UEI SLED_BA222F988CE579E3. It has been awarded $225,000 across 1 federal contract. Primary work spans In-Vitro Diagnostic Substance Manufacturing. Top awarding agencies include Pretrial Services.

Contact Information

Registration and classification details

Registration

UEI Code

SLED_BA222F988CE579E3

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

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Award Analytics & Distribution

Awards by Agency

Pretrial Services$225.0K100%

Awards by NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing$225.0K100%

Awards by Agency Over Time

Awards by Place of Performance

Open opportunities in MICROGENICS CORPORATION Fremont CA USA's top NAICS codes and agencies

65--Special Notice of Intent to Sole Source Award

It Services Fws

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TEST KIT, CORONAVIRUS DThe contract specifies the procurement of Abbott BinaxNOW COVID-19 Antigen Self Test kits for over-the-counter, at-home use, with each case containing twelve kits and each kit providing two tests. The test kits must be stored between 2 and 30 degrees Celsius and have a non-extendable shelf life of 12 months, with no more than one month elapsed from the date of manufacture to the date of delivery to the government. All packaging and labeling must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and each unit must be sealed in a suitable container to protect against damage, with exterior shipping containers ensuring safe, cost-effective delivery to the specified FPO address. Labels must clearly indicate the date of manufacture, expiration date, and contract or lot number. Technical and quality requirements are governed by the DLA Master List, and the item is subject to applicable defense information and packaging standards. The procurement is under contract SPE2DS-26-T-255U with a single case ordered, a 20-day delivery timeline, and primary contact information provided for coordination.

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TEST KIT, CHLAMYDIA TRAThis contract is for the procurement of a qualitative direct immunofluorescence test kit designed to detect Chlamydia trachomatis in human urogenital and ocular specimens, as well as to confirm the presence of Chlamydiae in cell cultures. The kit includes two positive control slides, mounting fluid, and the specific Chlamydia test reagent, ensuring accurate and reliable results for diagnostic purposes. The National Stock Number is 6550-01-725-3600, with a quantity of two kits requested under purchase request number 7017563729, and delivery is required within five days after order placement. The solicitation, identified as SPE2DS-26-T-257E, was posted on July 21, 2026, with a response deadline of July 27, 2026, and is categorized under NAICS code 325413 for pharmaceutical and medicine manufacturing. It is issued by the Department of Defense through the Medical Supply Chain MD Surg FSF, indicating federal procurement for military or veteran healthcare needs. The point of contact for inquiries is Mary-Kathryn Donahue, reachable via phone or email, and the contract is being managed through the DIBBS platform for government procurement activities.

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TRICHROME STAINING SETThe TRICHROME STAINING SET is a histological reagent kit designed for tissue differentiation, containing 250 mL of Wheatley trichrome stain, three 250 mL bottles of 70% ethanol, 250 mL of acid ethanol 90%, two 250 mL bottles of 95% ethanol, two 250 mL bottles of xylene-S, and five 0.75 mL ampules of Lugol’s iodine. The product must be stored in its original container at room temperature and is sold as a single unit. It is classified as a TYPE I (CODE F) item with a strict non-extendable shelf life of six months, requiring that no more than three weeks have passed from the date of manufacture to the date of delivery to the government. All packaging and labeling must comply with Medical Marking Standard No. 1, which supersedes MIL-STD-129, and must include the date of manufacture, expiration or retest date, contract number, and lot number in accordance with MMS1C guidelines. The item must be packaged in sealed unit containers that protect against damage and shipped in commercial exterior containers suitable for safe delivery via common carrier at the lowest rate to the specified delivery point in Williamsburg, Virginia. The procurement is governed by DLA’s master list of technical and quality requirements, packaging standards, and removal protocols for government identification on non-accepted supplies, with the solicitation issued under contract number SPE2DS-26-T-258J and NSN 6550-01-710-7934, with a required delivery within five days of award.

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CHIP, HYDROGEN PEROXThe contract specifies the procurement of a single unit of a hydrogen peroxide test chip designed for use with a CMS analyzer, containing ten measurement capillaries pre-filled with a substance-specific reagent detection system capable of measuring concentrations between 0.20 and 2.0 parts per million, sufficient for ten tests. The item is identified by NSN 6550-01-530-8328 and is governed by the solicitation SPE2DS-26-T-254T, with a required delivery within 20 days of award. The product must comply with strict technical and quality requirements referenced in the DLA Master List of Technical and Quality Requirements, including packaging standards detailed in DLA Packaging Requirements for Procurement. All units must be packaged commercially in sealed containers capable of preventing damage and must be shipped in compliant exterior containers suitable for safe delivery at the lowest freight rate to Joint Base Andrews, Maryland. Shelf-life is strictly limited to 12 months from the date of manufacture, with no extensions permitted, and no more than one month may have elapsed between manufacturing and government delivery. Labeling must conform to Medical Marking Standard No. 1, replacing all references to MIL-STD-129, and must include the date of manufacture, expiration date, contract number, and lot number. The item qualifies as a Type I (Code H) item under SPE2DS-26-T-254T, and all labels and packaging must adhere to the latest revision of MMS1C. Bidders are required to provide the source and part number being supplied, and the product is subject to potential coverage of defense information. The acquisition is for federal use under the Department of Defense, with point of contact information provided for inquiries.

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CONTROL, BLOOD CHEMIThe contract pertains to the procurement of CONTROL, BLOOD CHEMISTRY reagent, specifically Level 2 control reagent for use with i-STAT PT Plus cartridges on the i-STAT 1 analyzer system, with a unit of issue of BX containing 10 vials of 1.0 mL each. The item is identified by NSN 6550-01-725-6872, with a total quantity of 6 BX required under solicitation SPE2DS-26-T-237E, and delivery must be completed within five days of order placement at a destination point in Camp Lejeune, NC. The product requires refrigerated storage between 2 to 8 degrees Celsius (36 to 46 degrees Fahrenheit) and must not be frozen. It carries a strict 12-month shelf life that is non-extendable, with no more than one month allowed to have passed from the date of manufacture to the date of delivery to the government. Labeling must include the date of manufacture, expiration or retest date, and contract or lot number in accordance with the latest revision of Medical Marking Standard No. 1 (MMS NO. 1), which supersedes MIL-STD-129 for all medical acquisitions. Packaging must conform to commercial standards, utilize protective unit containers and exterior shipping containers suitable for safe transport at the lowest carrier rate, and meet DLA Packaging Requirements for Procurement (RP001) and MIL-STD-2073-1E for packaging data coding and preservation methods. All materials must be marked in compliance with MMS NO. 1, including 2D barcode specifications for supply chain traceability. This procurement is governed by numerous federal acquisition regulations and defense-specific requirements, including the DLA Master List of Technical and Quality Requirements (RA001), which identifies technical standards referenced by R or I numbers, and the applicability of Covered Defense Information under RD003. The contract mandates compliance with FAR and DFARS clauses relating to safeguarding controlled information (252.204-7012), combating trafficking in persons (52.222-50), employment eligibility verification (52.222-54), sustainable products (52.223-23), and hazard communication with required Safety Data Sheets (52.223-3). Payment must be processed electronically via Wide Area WorkFlow (

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Supplier of Hektoen Enteric Agar Culture MediaThe contract solicits the supply of Hektoen Enteric Agar culture media in packaged form, requiring full compliance with FDA Good Manufacturing Practices, MMS No. 1, and hazardous materials labeling standards. All products must be properly packaged, accurately labeled, and shipped using methods designated by WAWF to ensure regulatory adherence and safe delivery. The media is intended for use in medical and laboratory settings under the purview of the Department of Defense’s Medical Supply Chain. The solicitation was posted on July 20, 2026, with responses due by July 27, 2026, and is structured as a subcontract under NAICS code 325413 for pharmaceutical and biological product manufacturing. Performance is scheduled for FPO, ZIP 09566-4008, with no specific point of contact listed and no set-aside classification applied.

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NEW METHYLENE BLUE N SThis is a two-component reagent pack designed for the quantitative determination of reticulocytes in whole blood specimens using hematology analyzers. The kit includes Reagent A, a staining solution containing 0.06% w/v new methylene blue in a buffered formulation, and Reagent B, a clearing solution comprising 0.15% w/v sulfuric acid with stabilizers. The reagents are packaged as one 380 mL bottle of Reagent A and one 1,900 mL bottle of Reagent B, and must be stored between 36°F and 86°F (2°C to 30°C). The product has a non-extendable shelf life of 12 months, with no more than one month allowed to have elapsed from the date of manufacture to the date of delivery to the government. Packaging must comply with Medical Marking Standard No. 1, replacing all prior references to MIL-STD-129, and all items must be marked accordingly. The item is classified as a TYPE I (CODE H) medical supply under shelf-life requirement RS011, and government identification must be removed from non-accepted supplies per RQ011. Technical and quality requirements referenced in this contract are drawn from the DLA Master List of Technical and Quality Requirements. The procurement is under solicitation SPE2DS-26-T-250H, with a purchase request for 10 units to be delivered within 20 days of award, to the military postal address FPO 09566-4008.

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FECAL SPECIMEN COLLThe fecal specimen collection and transportation kit is a specialized parasitology kit designed for the collection, preservation, and transport of stool samples for the detection of intestinal parasites. Each kit contains a screw-cap vial with a built-in collection spoon and is color-coded for easy identification. The kit is a two-vial system, employing ZN-PVA and 10% formalin media to maintain sample integrity during transit and storage. Kits must be stored at room temperature between 15°C and 30°C, avoiding excessive heat or cold. The unit of issue is a package of ten kits, marked in accordance with Medical Marking Standard No. 1, superseding MIL-STD-129. The item has a non-extendable shelf life of 24 months, with no more than three months elapsed from manufacturing to government delivery. Technical and quality requirements referenced in the contract are governed by the DLA Master List of Technical and Quality Requirements, and packaging must comply with DLA procurement standards. The item is identified by NSN 6550-01-737-1200 and is subject to a delivery requirement of ten days after award.

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CULTURE MEDIA, HEKTOThis contract specifies the procurement of HEKTOEN ENTERIC AGAR culture media for the isolation of Salmonella and Shigella species, featuring a moderately selective formulation that enables differentiation through H2S production, resulting in black-centered colonies, and a high lactose content to prevent delayed fermentation. The medium is light beige in color and must be stored under refrigeration between 2 to 8 degrees Celsius, with no freezing allowed. Each unit of issue consists of 100 packages per PG, with a total order of 2 PG. The item is classified as a TYPE I (CODE C) medical product with a non-extendable shelf life of three months, requiring that no more than 13 days have passed from the date of manufacture to the date of government delivery. All packaging must comply with Medical Marking Standard No. 1, replacing MIL-STD-129, and must clearly label the date of manufacture, expiration or retest date, and contract or lot number according to the latest revision of MMS1C. The solicitation, identified as SPE2DS-26-T-250P, is issued by the Department of Defense through the Medical Supply Chain MD Surg FSF, with a response deadline of July 27, 2026, and a required delivery within 20 days of award. The NSN is 6550-01-737-5668, and the purchase request number is 7017324176. Technical and quality requirements are incorporated by reference from the DLA Master List of Technical and Quality Requirements, and the item falls under NAICS code 325413. Covered defense information may apply, and all supplies must adhere to DLA packaging standards, including the removal of government identification from non-accepted supplies. Point of contact for inquiries is Anh Lam, reachable via email and phone provided.

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CULTURE MEDIUM, XYLOThis contract specifies the procurement of Xylose Lysine Deoxycholate Agar culture medium, a selective and differential medium used for the isolation of gram-negative enteric pathogens. The product is supplied in units of 100 plates per package, each plate measuring 12mm by 85mm, and requires refrigerated storage between 2 to 8 degrees Celsius with no freezing allowed. The item has a strict two-month shelf life that is non-extendable, and delivery to the government must occur no later than nine days after the date of manufacture. Packaging must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and all labeling and marking requirements must be followed as defined by this standard. Technical and quality requirements referenced under RA001 are governed by the DLA Master List of Technical and Quality Requirements, with applicability controlled by the solicitation or award date depending on acquisition size. The item is classified as a TYPE I CODE B item under shelf-life requirement RS004, and covered defense information may apply as noted under RD003. Packaging must also adhere to DLA packaging standards as specified in RP001, and government identification must be removed from non-accepted supplies per RQ011. The National Stock Number is 6550-01-737-4202, with a single unit of purchase ordered under purchase request 7017325200, and delivery is due within 20 days after award. The solicitation, issued under SPE2DS-26-T-250E by the Department of Defense’s Medical Supply Chain, was posted on July 20, 2026, with responses due by July 27, 2026.

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CONTROL SET, COMPLETE BThis contract is for the procurement of a Complete Blood Count Control Set, specifically designed to ensure the accuracy and reliability of reticulocyte counts and related parameters on hematology analyzers. The product consists of three levels of control material, with four vials per level, each containing 3.5 mL, for a total of 12 vials per kit. The item is designated as a TYPE I (CODE C) medical supply with a non-extendable shelf life of three months, requiring that no more than 13 days have elapsed from the manufacturing date to the delivery date to the government. Refrigeration between 2 and 8°C is mandatory for storage. Each unit must be sealed in a commercially appropriate container to prevent damage and shipped in exterior packaging that ensures safe delivery by common carrier at the lowest cost to the designated delivery point. Labeling must comply with Medical Marking Standard No. 1, including the date of manufacture, expiration date, contract number, and lot number, and all markings must adhere to the latest revision of MMS1C. The NSN is 6550-01-625-1255, and the order is for five kits under solicitation SPE2DS-26-T-250A, with a delivery deadline of 20 days after award. Technical and quality requirements referenced in the DLA Master List apply, and the item is subject to Defense Information protections. Packaging, labeling, and marking must conform entirely to commercial standards as specified in the procurement documentation, superseding all prior military standards.

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Dual Path Platform (DPP) Vet Tuberculosis (TB) Assay KitsThe United States Department of Agriculture’s Animal and Plant Health Inspection Service is seeking 600 Dual Path Platform (DPP) Vet Tuberculosis Assay kits for use in the Federal Bovine Tuberculosis Eradication Program. These single-use immune-chromatographic tests are designed to detect antibodies to Mycobacterium bovis in cervid samples and serve as the official diagnostic tool for tuberculosis in conjunction with other methods. The solicitation, identified as 12639526Q0229, was posted on July 17, 2026, with responses due by July 29, 2026, and no set-aside provisions apply. The contract falls under NAICS code 325413 and is managed by the Department of Agriculture through the Minneapolis office, with performance expected in Iowa. Primary contact for inquiries is Julia Lackey, reachable via email or phone, and full details are available through the provided SAM.gov link.

Mrpbs Minneapolis Mn

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ProteinSimple Maurice consumablesThe FDA is seeking information from potential suppliers regarding consumables and materials required for the Protein Simple Maurice system, model Maurice – OBM, serial number KF-1804, which is used in regulatory research and testing for complex biopharmaceuticals. This sources sought notice, identified by solicitation number 75F40126SSN133285, was posted on July 17, 2026, with a response deadline of July 24, 2026, at 7:00 PM Eastern Time. The procurement falls under NAICS code 325413, indicating classification within the pharmaceutical and biological product manufacturing sector. The requesting organization is the FDA Office of Acquisition and Grant Services under the U.S. Department of Health and Human Services, located in Rockville, Maryland, with Suzanne Martella listed as the primary point of contact for inquiries. The place of performance is not specified, but the equipment is in use at FDA facilities, and responses are expected to address the technical specifications and availability of compatible consumables. This is not a formal solicitation for award but a request for market research to inform future procurement planning.

FDA Office Of Acq Grant Svcs

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Pharmaceutical Packaging and Labeling ServicesThe contract involves the labeling and packaging of Tramadol tablets in strict accordance with Defense Logistics Agency requirements, ensuring all products are marked with National Stock Number, National Drug Code, Commercial and Government Entity code, and Transaction Control Number for full traceability and regulatory compliance. The work must meet precise military and pharmaceutical standards to support the Department of Defense’s supply chain integrity. The contract is classified as a subcontract under NAICS code 325413, which pertains to pharmaceutical preparation manufacturing, and it was posted on July 16, 2026, with the associated contract number SPE2DX25D8022 and delivery order SPE2D926F7378. All activities are governed by DLA’s directives to maintain product authenticity, security, and compliance throughout the packaging process, with no specific place of performance or point of contact provided in the documentation.

Defense Logistics Agency

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REFERENCE STANDARDThe contract pertains to a Reference Standard Set containing Phenobarbital calibrators, specified as six levels per package, requiring refrigerated storage between 2 to 8 degrees Celsius and prohibition against freezing. Each package, identified as one PG unit, contains six individual calibrators. The item is governed by stringent technical and quality standards referenced in the DLA Master List of Technical and Quality Requirements, with compliance tied to the version in effect at the time of solicitation or award. It is subject to DLA packaging and medical marking requirements, specifically the Medical Marking Standard No. 1, which supersedes MIL-STD-129 and mandates proper labeling with the date of manufacture, expiration or retest date, contract number, and lot number. Shelf life is strictly limited to six months from manufacture with no extensions permitted, and no more than three weeks may have passed from the date of manufacture to the date of delivery to the government. All packaging must comply with commercial standards, ensuring protection from damage and suitability for safe transportation via common carriers at the lowest cost to the designated delivery point in FPO, 09566-4008. The item, identified by NSN 6550-01-670-6710, is part of a solicitation issued on July 16, 2026, with responses due by July 22, 2026, and delivery required within 20 days of award. The contracting office is the Department of Defense’s Medical Supply Chain, and inquiries are to be directed to Mary-Kathryn Donahue.

MEDICAL SUPPLY CHAIN MD SURG FSF

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Notice of Intent to Sole Source Reagents, calibrators and controls to be used in conjunction with the VITROS 3600 Immunodiagnostic system, manufactured by QuidelOrtho Sales Company, LLCThe U.S. Centers for Disease Control and Prevention Office of Acquisition Services intends to award a sole source contract to QuidelOrtho Sales Company, LLC for the supply of reagents, calibrators, and controls compatible with the VITROS 3600 Immunodiagnostic system. This procurement is authorized under federal acquisition regulations that permit simplified procedures for commercial items and sole source actions, with the NAICS code 325413 and PSC 6550 identifying the product category. No formal solicitation exists, and responses to this notice are not proposals or quotations but expressions of interest aimed at helping the government determine whether competition is feasible. Interested parties must submit detailed technical and pricing information by 5:00 PM ET on July 31, 2026, to qty0@cdc.gov, and must ensure timely delivery. The government retains full discretion to proceed without competition based on the feedback received. The action is managed by the CDC under the Department of Health and Human Services, with the primary point of contact being Brian Swann at 678-475-4520 or bswann@cdc.gov. The contract will be performed in Atlanta, Georgia, and no set-aside provisions apply. While this notice is not a request for bids or a binding commitment, submissions will inform the agency’s decision on whether to pursue a competitive process. The government will not consider any unsolicited proposals received after the deadline and will not entertain inquiries via phone or email regarding this notice. All submissions must be sent via email to the specified address, and submitters assume full responsibility for timely delivery and completeness of information.

CDC Office Of Acquisition Services

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Supply of Qiagen PCR and DNA/PCR Cleanup ReagentsThe contract is for the supply of Qiagen PCR reagents and DNA/PCR cleanup kits specifically designated for use with the QIAcube HT platform in genetic data processing operations. These materials are essential for enabling accurate and efficient DNA extraction, amplification, and purification tasks critical to the agency’s genetic analysis workflows. The procurement is structured as a subcontract under the North American Industry Classification System code 325413, indicating it relates to pharmaceutical and biological product manufacturing. The solicitation was posted on July 16, 2026, with a response deadline of July 24, 2026, at 2:00 PM, allowing suppliers a limited window to submit proposals. The contracting entity is the South Carolina office of the Department of Natural Resources, though specific location details such as city, state, or address are not provided. The opportunity is accessible via an online portal linked through the South Carolina procurement system, and no set-aside provisions or organizational type restrictions are specified, suggesting open competition among qualified vendors.

Department Of Natural Resources

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