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This Government Contract opportunity from Department Of Defense was posted on May 31, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Medical Device Manufacturing and Assembly

Closed
Federal

Contract Overview

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This contract involves the full manufacturing process, assembly, and quality control of pressure infusor devices in accordance with DLA, FDA, and shelf-life standards. The scope includes all necessary steps from production through final packaging and labeling to ensure compliance with regulatory and performance requirements. The contract is a subcontract under the Department of Defense's Medical Supply Chain MD Surg FSF agency and falls under the NAICS code 339112, which pertains to surgical and medical instrument manufacturing. The place of performance is Annville, with the specified ZIP code 17003-5003. The solicitation was posted on May 31, 2026, and responses are due by June 8, 2026. Though details such as the solicitation number and set-aside status are not provided, the contract clearly emphasizes adherence to strict quality and regulatory standards vital for medical device production. The full scope ensures that all manufactured devices meet required safety, functionality, and labeling specifications before delivery.

General Info

Manufacture, assemble, and quality control pressure infusor devices per DLA, FDA standards in Annville.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

339112 - Surgical and Medical Instrument Manufacturing View NAICS

Place of Performance

ANNVILLE, PA, 17003-5003, 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 CHAIN MD SURG FSF
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
Office AddressN/A
ContactsNo contact information available

Full Description

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Full manufacturing, assembly, and quality control of pressure infusor devices per DLA, FDA, and shelf-life requirements, including final packaging and labeling.