- Gap review, remediation roadmap, and implementation support
- Policy package, evidence mapping, and submission prep
- Designed for primes and subs across non-tech and tech work
SPE2DE26R003 | Medical ECAT Request for Information
Federal opportunity from DIBBS • DEPT OF DEFENSE.DEFENSE LOGISTICS AGENCY.TROOP SUPPORT MEDICAL.DLA TROOP SUPPORT. Place of performance: United States. Response deadline: May 11, 2026. Industry: NAICS 339112.
CMMC support options for this DoD solicitation
As DoD CMMC rollout expands, approximately 80%+ of DoD solicitations are expected to include cybersecurity/CMMC requirements, including many non-tech scopes.
- Structured checklist, AI guidance, and progress tracking
- Build evidence and controls with clearer next-step workflows
- Ideal for teams that want speed plus affordability
Market snapshot
Awarded-market signal for NAICS 339112 (last 12 months), benchmarked to sector 33.
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Applicable Wage Determinations
SAM WDOL references matched to this opportunity's location and scope language.
Point of Contact
Agency & Office
More in NAICS 339112
Description
DIBBS RFQ listing for solicitation SPE2DE26R003. Item or requirement: Medical ECAT Request for Information. Synopsis: The Defense Logistics Agency is the Department of Defense's largest logistics combat support agency, providing worldwide logistics support in both peacetime and wartime to the military services. The purpose of this Request for Information is the gain further knowledge of potential Small Business Manufacturing sources who can provide medical/surgical supplies and equipment similar to those listed on the attached document. If a Vendor wishes to provide an alternate item to those listed, it is the Vendor’s responsibility to provide manufacturer data, which clearly describes the characteristics and features of the alternate item being offered. Data submitted shall cover interchangeability and other characteristics of the offered products. A cross reference list comparing the features and capabilities of the alternate item offered to the exact item listed is required. The cross reference list shall be sufficient to enable the Government to determine whether the offered alternate product is equal to the product cited. The cross reference list shall also include the production capacity of the manufacturing source and the country of origin. All items must be manufactured by Buy American Act (BAA) qualified countries. All products offered must be Food and Drug Administration (FDA) approved. Small Business distributors and/or manufacturers shall provide a capability statement. The Review the DIBBS record and linked PDF for NSN details, packaging, clauses, and submission instructions.
DIBBS / DLA Details
Files
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BidPulsar Analysis
A practical, capture-style breakdown of fit, requirements, risks, and next steps.
FAQ
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It summarizes awarded-contract behavior for the opportunity’s NAICS and sector, including a recent pricing band (P10–P90), momentum, and composition. Use it as context, not a guarantee.
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