SRS MEDICAL SYSTEMS, INC.

SRS MEDICAL SYSTEMS, INC. specializes in the design, manufacturing, and delivery of precision surgical and medical instrumentation, with demonstrated expertise in urological diagnostic systems. Their recent award for the EASYFLO UROFLOW SYSTEM underscores a focused capability in developing clinically validated, flow-measurement devices used for non-invasive assessment of lower urinary tract function. The company leverages advanced electro-mechanical engineering, sensor integration, and biomedical signal processing to produce reliable, FDA-regulated medical devices that meet strict clinical and regulatory standards. Their technical proficiency includes embedded firmware development, fluid dynamics modeling, and compliance with ISO 13485 quality management practices for medical device manufacturing. The contractor has established a direct working relationship with the Department of Veterans Affairs, providing specialized urological diagnostic equipment tailored to veteran healthcare needs. This engagement suggests a track record of meeting VA’s clinical procurement requirements for outpatient urology clinics and veterans’ medical centers, with an emphasis on durable, user-friendly devices that support long-term patient monitoring and diagnostic accuracy. SRS MEDICAL SYSTEMS operates primarily within NAICS 339112, focusing on the manufacturing of surgical and medical instruments—specifically diagnostic devices used in urology. Their market positioning centers on niche, high-precision instrumentation rather than broad medical equipment lines, distinguishing them as a specialized supplier to clinical environments requiring reliable, low-maintenance diagnostic tools. As a small business structured as a 2L entity based in Chelmsford, Massachusetts, SRS MEDICAL SYSTEMS maintains a lean, agile operational model suited for specialized medical device production. While no federal certifications are listed, their ability to deliver a complex medical device to a federal agency confirms adherence to applicable regulatory and quality frameworks required for government procurement. Their geographic proximity to major biomedical hubs supports collaboration with clinical partners and regulatory experts in the Northeast corridor.