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Manufacturing of Sterile Tracheal Tubes (Murphy Design)

Active
Federal

Contract Overview

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

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This subcontract involves the manufacturing of sterile, disposable, and individually packaged nasal and oral tracheal tubes for prime contractors supporting DLA Troop Support Medical Supply Chain projects. The tubes must be fabricated from plastic polyvinyl according to Murphy design and E12 specifications, featuring a beveled tip and cuff with a 28 FR size and 7 mm internal diameter. Production must take place within cleanroom facilities using specialized sterilization equipment to ensure the delivery of medical-grade sterile products. To qualify for this contract, the manufacturer must maintain FDA registration, hold FDA 510(k) clearance, and demonstrate full compliance with Good Manufacturing Practices. The project is managed under the Department of Defense and is associated with NAICS code 339113, with the place of performance located in San Antonio, Texas.

General Info

Manufacturing sterile nasal and oral tracheal tubes for DLA in San Antonio, Texas.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

SAN ANTONIO, TX, 78226, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-27-T-1471.

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

View the prime solicitation

TUBE, TRACHEAL

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Timeline

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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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Manufactures sterile, disposable, individually packaged nasal and oral tracheal tubes for prime contractors on DLA Troop Support Medical Supply Chain projects. Fabricates tubes using plastic polyvinyl per Murphy design, E12 specification, with beveled tip and cuff (28 FR, 7 mm ID). Utilizes cleanroom facilities and sterilization equipment. Requires FDA 510(k) clearance, FDA registration, and GMP compliance. Delivers sterile tracheal tubes.

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