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This Government Contract opportunity from Department Of Defense was posted on May 19, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Medical Test Tube Supply

Closed
Federal

Contract Overview

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This contract involves the supply of 7 mL vacuum blood collection test tubes, which are classified as medical devices and must meet FDA and DLA standards. The procurement is managed by the Medical Supply Chain FSH under the Department of Defense, with performance required at an APO location bearing the postal code 09898. The solicitation was posted on May 19, 2026, with a response deadline set for May 26, 2026. It is classified as a subcontract under the NAICS code 325193, which pertains to manufacturing related to chemical manufacturing for medical purposes. The contract emphasizes compliance with regulatory standards essential for medical devices, ensuring that supplied test tubes are safe and effective for clinical use. Although no specific organization type or set-aside provisions are indicated, the scope of this solicitation is focused on supporting military or defense-related medical supply needs. The procurement process and further details are accessible via the Defense Logistics Agency’s bidding platform.

General Info

Supply of 7 mL FDA-compliant blood test tubes for DoD medical use, APO 09898 delivery.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIIN FSH

NAICS

325193 - Ethyl Alcohol Manufacturing View NAICS

Place of Performance

APO, AE, 09898, US

Set-Aside

NONE

Documents

(0)

No documents available

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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
Office AddressN/A
ContactsNo contact information available

Full Description

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Supply of 7 mL vacuum blood collection test tubes compliant with FDA and DLA standards, classified as medical devices.