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

Supply of Masimo MightyStar RX Pulse Oximeters

Closed
Federal

Contract Overview

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This subcontract involves the supply of Masimo MightyStar RX pulse oximeters to prime contractors supporting Department of Defense DLA supply contracts. These specialized devices are designed for patient movement environments and must be capable of measuring perfusion index, SpO2, and pulse rate while operating on two AAA alkaline batteries. The contract requires the delivery of two units to a designated inspection point in FPO 96661. To ensure medical safety and quality, all supplied equipment must maintain FDA 510(K) clearance and strictly adhere to GMP standards and Regulation 870.2700 Class II. The procurement is managed under NAICS code 423450 through the Medical Supply Chain MD Surg FSF agency.

General Info

Supply two FDA-cleared Masimo MightyStar RX pulse oximeters to DoD DLA prime contractors.

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

Place of Performance

FPO, AP, 96661, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-379K.

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

View the prime solicitation

OXIMETER, PULSE

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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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Supplies Masimo MightyStar RX pulse oximeters for prime contractors on DLA supply contracts. Provides devices capable of measuring pulse rate, SpO2, and perfusion index designed for patient movement environments. Supplies items compatible with 2 AAA alkaline batteries. Requires FDA 510(K) clearance and compliance with Regulation 870.2700 Class II and GMP standards. Delivers two pulse oximeters to the destination inspection point.

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