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This Sources Sought opportunity from Department Of Defense was posted on July 23, 2025. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Gas Chromatograph with Mass Spectrometer (GC/MS)

Closed
PANHCA-25-P-0000-025641Federal

Contract Overview

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

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General Info

NAICS

339112 - Surgical and Medical Instrument Manufacturing

Place of Performance

Landstuhl, DE-RP, 09180, DEU

Set-Aside

NONE

Documents

0

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Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → W40M Mrco Europe
Contacts2 people available
OfficeAPO, AE, 09180-0402, USA
Office AddressAPO, AE, 09180-0402, USA
Contacts

Full Description

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THIS IS A SOURCES SOUGHT/REQUEST FOR INFORMATION ONLY. This is not a Solicitation Announcement, nor is it a Request for Proposal. This request does not obligate the Government in any contract award. The USAHCA - Medical Readiness Contracting Office Europe-USAHCA-MRCO-EUR is issuing the sources sought synopsis as a means of conducting market research to identify parties having an interest in and the resources to support the requirement for Gas Chromatograph with Dual Electron Capture Detector. The result of this market research will contribute to determining the method of procurement. The applicable North American Industry Classification System (NAICS) code assigned to this procurement is 339112 (Surgical and Medical Instrument Manufacturing) with business size standard 1,000 Employees. PSC code is 6630 - Chemical Analysis Instruments. The anticipated delivery 45 days after contract award. The delivery address: Regional Landstuhl Medical Center Landstuhl, Germany SALIENT CHARACTERISTICS Brand Name or Equal Gas Chromatograph with Mass Spectrometer (GC/MS) with the ability to screen drinking water and food samples for a wide array of prominent and emergent organic pollutants simultaneously. - Data acquisition and processing software to control instrument and process data. - The sample inlet should have a split/split less injection (SSL). - The system must have an integrated compartment with capability for at least 2 columns and capability for addition of additional/alternate detector. - The instrument requires a high sensitivity electron ionization source with instrument detection level (IDL) ?1.5 fg octafluoronaphthalene (OFN). - Libraries/Database information to include 40CFR organic contaminants and emerging - Instrument and software capable of interfacing with a purge and trap system for analysis of EPA 524.4. - The instrument should come with an autosampler capable of interfacing with the instrument software and injecting a range of 1-10 uL sample. If you are interested in participating in this requirement and/or your organization has the potential capacity to provide, please submit the following to the Point of Contacts (POC) information listed below: 1. Name and Address of your Firm 2. Point of Contact (name/phone/email) 3. Company website 4. Unique Entity identifier (UEI) number 5. Commercial and Government Entity (CAGE) code 6. Capability statement -

More opportunities from Department Of Defense → W40M Mrco Europe

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NAICS: 325413
Federal
Blood Chemistry Testing - Cost Per Reportable Result
Solicitation # W9114F-26-Q-A009
The Medical Readiness Contracting Office-Europe is soliciting a Fixed-Price Indefinite Delivery/Indefinite Quantity contract for one automated chemistry analyzer and associated consumables to support the laboratory mission at the U.S. Army Health Clinic in Vicenza, Italy. Under a Cost Per Reportable Result pricing structure, the successful offeror will provide all new equipment, reagents, consumables, controls, and necessary maintenance. The contract includes a two-month phase-in period from January 2, 2026, to February 28, 2026, followed by an ordering period from March 1, 2026, through December 31, 2030. The estimated annual clinical chemistry workload is 42,595 tests. Technical requirements specify that the analyzer must be FDA-approved, capable of measuring analytes from a 300-microliter sample, and equipped with an uninterruptible power supply providing seven minutes of power. The system must have a current Authorization to Operate for interfacing with the Laboratory Information System and comply with the Risk Management Framework for DOD IT. The contractor is responsible for providing initial on-site operator training in English and ensuring all reagents are delivered at the proper storage temperature. Award will be based on the Lowest Price Technically Acceptable evaluation process under Simplified Acquisition Procedures, with the solicitation open for full competition under NAICS code 325413.
In-Vitro Diagnostic Substance Manufacturing

POSTED

12 months ago

DEADLINE

N/A
View Details

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