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Accepting bidstenderUnited States

Steritest Symbio ISL 2 System Pump-Brand Name and Equal (BNE)

Issued by HEALTH AND HUMAN SERVICES, DEPARTMENT OF · FOOD AND DRUG ADMINISTRATION · FDA OFFICE OF ACQ GRANT SVCS · via SAM.gov — US federal contract opportunities

Published
17 Sept 2026
Closes
22 Sept 2026, 20:00 UTC
Reference
FDA-RFQ-OC-2026-134494
Location
OH, United States
Sector
electronics-semiconductors

Details

HEALTH AND HUMAN SERVICES, DEPARTMENT OF · FOOD AND DRUG ADMINISTRATION · FDA OFFICE OF ACQ GRANT SVCS is soliciting Steritest Symbio ISL 2 System Pump-Brand Name and Equal (BNE). Solicitation number FDA-RFQ-OC-2026-134494. Classified under NAICS 334516 — Analytical Laboratory Instrument Manufacturing. Product/service code 6640 — LABORATORY EQUIPMENT AND SUPPLIES. Place of performance: OH, USA. Responses are due by 22 September 2026 20:00 UTC. Posted on SAM.gov, the US federal contract opportunities system; registration is required to bid.

Notice of Combined Synopsis/Solicitation. This is a combined synopsis/solicitation for commercial products or commercial services prepared in accordance with part 12. This announcement constitutes the only solicitation; quotes are being requested, and a separate written solicitation will not be issued. The NAICS for this requirement is: 334516. The government is not obligated to make an award. The Government is not obligated to pay costs incurred by the Contractor during quote preparation and quote submission.

Background

The National Forensic Chemistry Center (NFCC) in the Office of the Chief Scientist, Office of Specialty Laboratories & Enforcement Support, requires the purchase of one (1) One (1) Steritest Symbio ISL 2 Med US. The Steritest Symbio ISL 2 is designed to fit with the round isolator cut outs and can be installed into the existing NFCC Getinge ISO-FLEX-R Isolator. The Steritest® Symbio ISL Pump is suitable for sterility testing of large and small volume parenteral solutions in glass or plastic bottles, collapsible bags, ampoules, and vials, pre-filled syringes, lyophilized and other soluble products in ampoules or vials, antibiotics in ampoules or vials, medical devices, and difficult-to-dissolve powders. This will not only enable the analysis of forensic and regulatory sterility samples but will also support the development of new methodology for the NFCC and FDA. Minimum Performance Requirements/Salient Characteristics: All of the following system requirements are minimum requirements. Equivalent requirements that differ from these minimum requirements shall be justified by the proposing vendor and evaluated by the NFCC prior to purchase.

  • The System shall have all new components, include all necessary hardware to operate with the following specifications:

System to shall be supplied with Steritest Symbio shipping case or equivalent System shall include Steritest Equinox Pressure Control Kit or equivalent System shall include Steritest Pump Footswitch or equivalent System shall include Steritest Symbio Hub Holder or equivalent Pump housing must be stainless steel and be compatible with Vaporized Hydrogen Peroxide decontamination cycle. Must be compatible with prefabricated hole in Getinge IsoFlex-R Isolator All components must be compatible with use within Getinge IsoFlex-R Isolator. Trade and Service Specifications

  • The system must be a newly manufactured unit, not used and refurbished or previously used for demonstration. The Government must be able to expect routine customer service and technical support to be available from the vendor during its lifecycle.
  • A minimum one (1) year warranty on all components
  • Including parts, labor, travel, telephone support, software updates with an option for yearly service agreements. The Contractor shall be responsible for the system during transit. All costs including parts, labor, travel, and other expenses necessary to repair any machine equipment will be borne solely by the contractor at no additional cost to the U.S. Government. Onsite installation and training. The contractor shall conduct one (1) training session for up to three (3) users on-site. The training shall provide a thorough demonstration of all system/solution functions, maintenance, data administration, and basic troubleshooting. The training may be completed on-site immediately after installation/set-up and on-site measurements demonstrating that no damage or misalignment issues arose during transportation and installation but shall be completed no later than 30 days after installation.
  • Unlimited free telephone, e-mail, and/or FAX technical support for one year.

Place of Performance:

US Food & Drug Administration National Forensic Chemistry Center 6751 Steger Dr. Cincinnati, OH 45237

Period of Performance:

Performance begins on the date of formal government acceptance and continues through the end of the manufacturer's warranty period. Quotes are due by email on or before September 22, 2025, by 4:00 P.M. (Eastern Standard Time) and should be sent to [contact details removed].

Context for bidders

We hold 26 notices from HEALTH AND HUMAN SERVICES, DEPARTMENT OF · FOOD AND DRUG ADMINISTRATION · FDA OFFICE OF ACQ GRANT SVCS, going back to August 202613 of them still open. They buy mostly in electronics-semiconductors, Financial & Professional Services and IT & Telecom. There are 922 open electronics-semiconductors tenders in United States. This one closes in 5 days.

Before you bid on this tender

A quick checklist to help you decide whether to bid and prepare a compliant submission for this electronics-semiconductors opportunity. Always verify the details on the official source.

  • Confirm the exact closing date and time (and time zone) on the official portal — deadlines are strict and can be revised by a corrigendum.
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  • Prepare any earnest-money deposit (EMD) or bid security and the required formats early; missing or wrongly-formatted documents are a common cause of rejection.
  • Note how bids must be submitted (online or physical), in what format, and whether a digital signature or portal registration is required.
  • Watch for corrigenda and clarifications right up to the deadline — requirements and dates can change.

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