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Hazardous Material Compliance & Labeling Support

Active

Federal

Contract Overview

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

AI Contract Overview

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The contract requires the provision of hazard warning labels and Safety Data Sheets for all hazardous components included in a medical device, ensuring full compliance with OSHA and DFARS regulations. This effort is aimed at safeguarding users and handlers by clearly communicating potential risks associated with hazardous materials, and must be executed with precision to meet federal safety and documentation standards. The work is performed under a subcontract arrangement managed by the Defense Logistics Agency on behalf of the Department of Defense, tied to NAICS code 541690 for other scientific and technical consulting services, with the requirement posted on June 26, 2026. Place of performance and specific delivery details are not disclosed, and all deliverables must align with the stringent compliance demands of the federal supply chain.

General Info

Provide OSHA and DFARS-compliant hazard labels and SDS for medical device components under DLA subcontract.

Agency

Department Of Defense → Defense Logistics AgencyView Agency

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS6T092K.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

VALVE, SURGICAL DRAI

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Timeline

PostedJun 26

subcontract

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Logistics Agency

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Defense → Defense Logistics Agency

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Office AddressN/A

ContactsNo contact information available

Full Description

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Provide hazard warning labels and Safety Data Sheets (SDS) for any hazardous components in the supplied medical device, in compliance with OSHA and DFARS requirements.

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