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This Government Contract opportunity from Department Of Defense was posted on May 27, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Transfer Pipet Supply

Closed
Federal

Contract Overview

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The contract involves the supply of precision transfer pipets specifically designed for specimen collection, emphasizing the necessity for sterile packaging to maintain product integrity and prevent contamination. The pipets must comply with technical standards set by the Defense Logistics Agency (DLA), ensuring they meet stringent quality and performance requirements for medical use. This subcontract has a response deadline of June 3, 2026, and is posted by the Medical Supply Chain FSH under the Department of Defense. The place of performance is specified as Beaufort, with the zip code 29902-6148. The procurement falls under the NAICS code 326299, which pertains to plastics product manufacturing, aligning with the nature of the transfer pipets involved.

General Info

Supply of sterile precision transfer pipets for medical use, meeting DLA standards, deadline June 3, 2026.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIIN FSHView Agency

NAICS

326299 - All Other Rubber Product ManufacturingView NAICS

Place of Performance

BEAUFORT, SC, 29902-6148, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DH-26-T-4091.

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

View the prime solicitation

SPECIMEN KIT, URINE

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIIN FSH
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIIN FSH
View Agency Profile
Office AddressN/A
ContactsNo contact information available

Full Description

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Supply of precision transfer pipets used in specimen collection, requiring sterile packaging and compliance with DLA technical standards.

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