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Medicinal Nebulizer Manufacturing

Active

Federal

Response Deadline09/22/2026, 05:00:00 PM UTC

Contract Overview

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

AI Contract Overview

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This subcontract involves the manufacture of medicinal nebulizers for prime contractors supporting Defense Logistics Agency supply contracts under the Department of Defense. Production must adhere to FDA Regulation 868.5630 Class II and Good Manufacturing Practices, utilizing medical-grade plastics and maintaining FDA 510(k) clearance. All products must be marked according to Medical Marking Standard No. 1 and possess a non-extendable shelf-life of 36 months. Finished devices are to be delivered in packaging of 50 units per case. The opportunity is categorized under NAICS code 339112 and is managed by the Medical Supply Chain MD Surg FSF. Performance is designated for FPO 09592, with a response deadline of September 22, 2026.

General Info

Manufacture FDA-compliant medicinal nebulizers for DoD supply contracts by September 22, 2026.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

339112 - Surgical and Medical Instrument ManufacturingView NAICS

Place of Performance

FPO, AE, 09592, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-445H.

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

View the prime solicitation

NEBULIZER, MEDICINAL

AI Contract Breakdown

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Timeline

PostedSep 16

subcontract

Response DeadlineSep 22

Submission deadline

Response Deadline

09/22/2026, 05:00:00 PM UTCin 6 days

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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

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Office AddressN/A

ContactsNo contact information available

Full Description

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Manufactures medicinal nebulizers for prime contractors on Defense Logistics Agency (DLA) supply contracts. Produces devices according to FDA Regulation 868.5630 Class II and Good Manufacturing Practices (GMP), ensuring a non-extendable shelf-life of 36 months. Marks products per Medical Marking Standard No. 1. Requires FDA 510(k) clearance and medical-grade plastics. Delivers finished nebulizers packaged in cases of 50 units.

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