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1. Siemens Healthcare Diagnostics Inc.

UEI: SLED_71B93F1E6A6A780D

1. Siemens Healthcare Diagnostics Inc. is a federal contractor, registered under UEI SLED_71B93F1E6A6A780D. It has been awarded $1,770,797 across 1 federal contract. Primary work spans In-Vitro Diagnostic Substance Manufacturing. Top awarding agencies include Naval Medical Logistics Command.

Contact Information

Registration and classification details

Registration

UEI Code

SLED_71B93F1E6A6A780D

Federal Contracting Overview

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

Key Performance Metrics

Awards Count

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Award Analytics & Distribution

Awards by Agency
Naval Medical Logistics Command$1.8M100%
Awards by NAICS
325413 - In-Vitro Diagnostic Substance Manufacturing$1.8M100%
Awards by Agency Over Time
Export
Awards by Place of Performance

Open opportunities in 1. Siemens Healthcare Diagnostics Inc.'s top NAICS codes and agencies

NAICS: 325413
New
SLED
FY26 FR0 DFS/PHL - Qiagen reagentsThe contract forecasts the procurement of Qiagen reagents for forensic science testing applications under the Fiscal Year 2026 budget cycle, managed by the Forensic Sciences division within the District of Columbia. This initiative is tied to laboratory operations requiring reliable molecular diagnostics reagents, likely supporting DNA analysis, sample preparation, or other forensic testing workflows essential to criminal investigations and evidence processing. While the solicitation number and procurement details are not yet available, the posting date indicates this is a future forecast with no set-aside provisions indicated, meaning the opportunity is open to all eligible vendors without geographic or size-based restrictions. The place of performance and organizational details remain unspecified, but the activity is centered within the District of Columbia’s forensic system, suggesting delivery and use will occur at state or local forensic laboratories. No point of contact information is provided at this stage, and the NAICS code, office address, and other typical contracting metadata are also absent, indicating this is an early-stage forecast meant for market research and vendor awareness. Interested suppliers should monitor the official DC contracting portal for future solicitations tied to this forecast, as detailed requirements, timelines, and ordering procedures will be released in subsequent procurement actions.
Forensic Sciences (DFS)

POSTED

1 day ago

DEADLINE

N/A
View Details
NAICS: 325413
New
SLED
FY26 FR0 DFS/PHL - Other Molecular Testing ReagentsThe contract forecast pertains to molecular testing reagents for fiscal year 2026 under the Forensic Sciences division of the District of Columbia, targeting laboratory needs related to forensic analysis. Although no solicitation number or NAICS code is provided, the reagents are intended for use in molecular diagnostic applications that support forensic investigations, likely including DNA profiling, pathogen identification, or other biological sample analysis critical to criminal justice and public safety operations. The forecast was posted on July 23, 2026, indicating an upcoming procurement opportunity, and the place of performance is within the District of Columbia, though specific location details are not enumerated. No set-aside preferences or organizational type designations are specified, suggesting the opportunity may be open to all eligible vendors without restrictions based on size, gender, veteran status, or other classifications. The point of contact information is omitted, and no physical address details are provided for either the agency or performance location, indicating this is a preliminary notice rather than a formal request for proposals. Interested parties are directed to the online portal for updates on future solicitation documents, which will likely include detailed technical specifications, delivery requirements, evaluation criteria, and submission deadlines.
Forensic Sciences (DFS)

POSTED

1 day ago

DEADLINE

N/A
View Details
NAICS: 325413
New
DIBBS
CALIBRATOR KIT, HAEMATOThe CALIBRATOR KIT, HAEMATOLOGY is a specialized reagent kit designed for calibrating UNICEL DXH COULTER cellular analysis systems used in hematology applications, with each unit containing 3.3 mL of calibrator. It is subject to strict technical and quality requirements as defined in the DLA Master List of Technical and Quality Requirements, and must comply with DLA packaging standards including the Medical Marking Standard No. 1, which supersedes MIL-STD-129. The item is classified as a Type I (Code A) shelf-life item with a non-extendable shelf life of one month, requiring that no more than four days pass between the date of manufacture and delivery to the government. All packaging must include the date of manufacture, expiration date, contract number, and lot number, in accordance with the latest revision of MMS1C. The calibrator must be stored and transported under refrigerated conditions between 2°C to 8°C (36°F to 46°F) and must not be frozen. Packaging must be commercial-grade, sealed, and designed to protect contents from damage during shipping, with exterior containers suitable for safe delivery via common carrier at the lowest cost. The product is associated with NSN 6550-01-625-1271 and is being procured under solicitation SPE2DS-26-T-262K, with a required delivery within five days after award, and bidders must clearly specify the source and part number being offered.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

3 days ago

DEADLINE

in 3 days
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NAICS: 325413
New
DIBBS
TEST KIT, CHLORIDE DThis contract is for the procurement of TEST KIT, CHLORIDE D, specifically CHLORIDE QUANTAB TEST STRIPS rated for a high range of 300 to 6000 mg/L, supplied in quantities of 40 strips per bottle, with one bottle required. The item is identified by NSN 6550-01-722-0245 and is subject to strict technical and quality standards referenced from the DLA Master List of Technical and Quality Requirements, which govern its specification and compliance. The product must meet commercial packaging requirements as defined for medical acquisitions, including sealed unit containers to prevent damage and shipping containers suitable for safe transport at the lowest carrier rate. All packaging and marking must adhere to Medical Marking Standard No. 1, superseding MIL-STD-129, and include mandatory labeling with the date of manufacture, expiration date, and contract or lot number in accordance with MMS1C. The item has a non-extendable shelf life of 24 months, and no more than three months may have elapsed between the date of manufacture and delivery to the government. Delivery is required within 20 days after award, with performance addressed to Hampton, Virginia, under contract number SPE2DS-26-T-261X issued on July 22, 2026, with responses due by July 28, 2026. Bidders must provide the source and part number being offered, and the supply is subject to DLA packaging requirements and the potential application of covered defense information regulations. All items must be marked for government use and comply with procedures for removal of government identification from non-accepted supplies. The procurement is managed by the Department of Defense’s Medical Supply Chain under the office of Marc Canalichio, with full technical and logistical specifications enforced by DLA Troop Support.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

3 days ago

DEADLINE

in 3 days
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NAICS: 325413
New
Federal
6640--LAB - ROCHE BENCHMARK ULTRA PLUS STAIN CPTThe Department of Veterans Affairs, through Network Contracting Office 2, intends to award a sole-source contract to Roche Diagnostics Corporation for proprietary reagent kits and consumables compatible with VA-owned Roche Benchmark Ultra Plus immunohistochemistry instruments. This action is justified under FAR 6.302-1 due to the technical exclusivity of the reagents, as no alternative suppliers can provide products that function with the existing VA equipment. The solicitation, identified by number 36C24226Q0827, was posted on July 22, 2026, with responses due by July 30, 2026, at 10:00 a.m. Eastern Time, submitted exclusively via email to the Contracting Officer, Aleta Jennette. The contract is for laboratory reagents essential to ongoing diagnostic operations, primarily at the James J. Peters VA Medical Center in Bronx, NY, though the final place of performance remains TBD. No competitive solicitation exists, and therefore no formal evaluation factors, pricing details, line items, or contract value have been established. The procurement is non-competitive, with no set-asides for small or socioeconomic businesses, and no socioeconomic certifications or UEI/CAGE codes for the vendor are provided. Packaging, marking, preservation, inspection, acceptance criteria, and invoicing methods are not specified, with assumed compliance to standard commercial practices for laboratory reagents. Contract administration oversight is limited to the Contracting Officer, with no designated COR, COTR, or PCO identified. The contracting office is located in Albany, NY, but administrative and performance functions are centered at the Bronx facility. No FAR clauses, special requirements, or representations from the offeror are included, as the document serves solely as a market research notice indicating intent to award without requiring formal proposals, quotes, or submissions other than expressions of interest. The acquisition is driven entirely by proprietary compatibility, with no alternatives available, rendering traditional contract elements such as pricing, delivery schedules, or payment terms unnecessary at this preliminary stage.
242-NETWORK Contract Office 02 (36C242)

POSTED

3 days ago

DEADLINE

in 5 days
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NAICS: 325413
New
Federal
Notice of Intent to Sole Source Serology DV-1-4 EDIII ReagentsThe Centers for Disease Control and Prevention plans to award a sole source firm fixed price contract to the University of North Carolina at Chapel Hill’s Microbiology & Immunology department for the custom production of biotinylated EDIII antigens specific to Zika virus and all four dengue virus serotypes. These antigens are essential for developing and validating serologic assays using streptavidin-based capture and multiplex immunoassay platforms, ensuring high sensitivity and specificity in distinguishing prior infections between dengue and Zika viruses. A HaloTag control antigen is also required to assess nonspecific binding and assay background, providing critical quality control for reagent performance. Commercial alternatives such as whole-virus antigens, full-length envelope proteins, NS1 antigens, and non-biotinylated EDIII constructs were evaluated but rejected due to their inability to meet technical requirements, including excessive cross-reactivity, incompatible tagging systems, inconsistent purity, or mismatched manufacturing methods that would compromise assay reproducibility and data comparability with existing validated protocols. The use of any substitute reagents would necessitate extensive additional optimization, bridging studies, and new validation efforts, leading to significant delays, increased costs, and potential disruption to ongoing laboratory operations. The selected supplier’s ability to produce these antigens with precisely defined sequences, consistent biotinylation, and standardized manufacturing processes is critical to maintaining continuity in the Dengue Branch’s serologic assay strategy. This procurement is authorized under FAR 6.103-1 (SAP) and 41 U.S.C. 1901, allowing for non-competitive award based on the unique technical specifications and absence of viable alternatives. While the notice invites public response, any submissions received by August 6, 2026, at 5 p.m. EST will be considered at the government’s sole discretion to confirm the necessity of sole source procurement, with all correspondence to be directed to iris.gonzalez@cdc.gov. The anticipated performance location is Atlanta, Georgia.
Centers For Disease Control And Prevention

POSTED

3 days ago

DEADLINE

in 12 days
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NAICS: 325413
New
Federal
65--Special Notice of Intent to Sole Source AwardThe U.S. Fish and Wildlife Service intends to award a sole source firm fixed price contract to Qiagen, LLC for proprietary genetic reagents and consumables essential to the Pacific Region Fisheries and Aquatic Conservation Program and the Abernathy Fish Technology Center. The requirement, classified under NAICS code 325413, involves specialized patented products that are critical to maintaining the integrity of genetic analysis workflows and supporting federally mandated species recovery plans. Qiagen is the exclusive manufacturer and distributor of these items, with no authorized resellers, and previous attempts to use alternative suppliers have yielded unreliable results that compromise mission-critical research. The contract value is expected to be at or below the simplified acquisition threshold of $350,000, authorized under FAR Part 12.102(a). This notice serves solely as an intent to award and does not constitute a solicitation, but interested parties may submit a written statement of capabilities demonstrating how competition would benefit the government. All submissions must be sent via email as a Microsoft Word or Adobe PDF attachment to Lawrence_aragon@ios.doi.gov by August 1, 2026, and must provide clear and convincing evidence supporting competitive procurement. No telephone inquiries or offers will be accepted, and respondents bear full responsibility for any costs incurred in preparing their submissions. The contracting office is located in Falls Church, Virginia, with the point of contact being Lorenzo Aragon.
It Services Fws

POSTED

3 days ago

DEADLINE

in 7 days
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