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This Government Contract opportunity from Department Of Defense was posted on October 1, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Chest Tube Insertion Kit Assembly and Sterile Packaging

Closed
Federal

Contract Overview

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This subcontract involves the assembly and sterile packaging of emergency chest tube thoracostomy kits for prime contractors supporting DLA Troop Support medical supply contracts. The selected provider is responsible for sourcing individual medical components, assembling them into single units, and vacuum-sealing each kit within a sterile pouch. All work must be performed in clean-room environments using specialized vacuum sealing equipment to ensure strict adherence to medical device sterility standards and FAR 52.219-1 regulations. The scope of work requires the delivery of 25 vacuum-sealed, sterile kits. This requirement is managed by the Department of Defense under the Medical Supply Chain MD Surg FSF agency, falling under NAICS code 339113. The solicitation was posted on October 1, 2026, with a response deadline of October 7, 2026.

General Info

Subcontract for assembly and sterile packaging of 25 emergency chest tube thoracostomy kits.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-27-T-0043.

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

View the prime solicitation

INSERTION KIT, CHEST TU

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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 CHAIN MD SURG FSF
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Assembles and packages sterile emergency chest tube thoracostomy kits for prime contractors on DLA Troop Support medical supply contracts. Sources individual medical components, kits them into a single unit, and vacuum-seals the kit in a sterile pouch using clean-room environments and vacuum sealing equipment. Must meet medical device sterility standards and FAR 52.219-1. Delivers 25 vacuum-sealed, sterile kits.

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Miguel
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Keith Deutsch
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