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Medical Device Sterilization Services

Active
Federal

Contract Overview

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The contract provides for the sterilization of Azur Coils and associated components using validated methods such as gamma radiation, ethylene oxide (ETO), or other approved techniques that meet current medical device regulatory standards. This service is critical to ensuring the safety and compliance of products used in medical applications, with all processes required to adhere to internationally recognized sterilization validation and quality control protocols. The work must be performed in accordance with applicable FDA and ISO guidelines to maintain the integrity and sterility assurance of the devices. This subcontract is issued under NAICS code 561990 for other support services and is managed by the Department of Veterans Affairs through the 250-NETWORK Contract Office 10 (36C250). The contract was posted on July 2, 2026, and the performance location is not specified. While no set-aside status or point of contact details are provided, all work must be executed in compliance with federal procurement regulations and medical device sterilization requirements, ensuring that delivered components are free from microbial contamination and ready for clinical use.

General Info

Sterilization of Azur Coils via gamma or ETO per FDA and ISO standards for medical device compliance.

Agency

Department Of Veterans Affairs → 250-NETWORK Contract Office 10 (36C250)View Agency

NAICS

561990 - All Other Support ServicesView NAICS

Place of Performance

OH

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

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subcontract

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → 250-NETWORK Contract Office 10 (36C250)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Veterans Affairs → 250-NETWORK Contract Office 10 (36C250)
View Agency Profile
Office AddressN/A
ContactsNo contact information available

Full Description

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Contract sterilization of Azur Coils or related components using gamma, ETO, or other validated methods compliant with medical device regulations.

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