How to Contact Medical Murray About a Medical Device Project

Updated

The site's primary path is its Contact Us call-to-action, which appears alongside the invitation to "get started" on a project. Medical Murray presents itself as a contract development and manufacturing organization (CDMO) for minimally invasive devices and implants, supporting work from concept through commercialization — so the most effective first message states which stage you're at (design, prototyping, testing, or manufacturing) and which device area applies. The site does not publish a direct email address, phone number, or contact form fields in the available material, so use the Contact Us link on medicalmurray.com as the entry point and be ready to describe your project in those terms.

What to include in your first inquiry

A useful inquiry maps directly onto the three service pillars the site names — Development, Testing, Manufacturing — and onto its core technology areas. Before writing, decide:

  • Stage: original design, problem-solving on an existing design, prototyping, verification/testing, or contract manufacturing.
  • Device category: complex catheters (vascular, gastrointestinal, urologic, other interventional), implants and delivery systems (covered stents and frames, bioabsorbables, textiles, sensors), or material technologies (ePTFE implants, covered stents and frames, catheter shafts).
  • Clinical market, if known: aortic, structural heart, neurovascular, cardiovascular, peripheral vascular, orthopedics, gastroenterology, or urology.

For example, a team with a catheter-shaft concept and no manufacturing partner would frame the message as: development and prototyping support for a peripheral vascular catheter, with a path toward assembly and testing. That single sentence tells the recipient which engineering group and which service line are relevant.

Checking fit before you reach out

Two site sections help you qualify the conversation in advance:

What to check Where Why it matters
Quality credentials Homepage credentials block: FDA Registered, ISO 13485 Certified, ISO/IEC 17025:2017 Accredited Confirms the quality and testing infrastructure relevant to a regulated device program
Technical scope "Our Core Technologies" (Complex Catheters, Implants, Material Technologies) Lets you name the specific capability you need rather than a generic request
Working style and lessons Newsroom & Resources blog, e.g. posts on rapid prototyping and verification testing Useful context on how the firm approaches early-stage build-and-learn work and test planning

The blog items are worth a skim before contacting: the rapid prototyping piece argues against jumping straight into detailed CAD of the "real" product, and the verification testing piece flags treating verification as a late-stage activity as a common mistake. Referencing that framing in your inquiry signals you've thought about sequencing.

Events as an alternative first contact

The site lists trade events, including MD&M West 2026 in Anaheim, California, Booth #1521, February 3–5, 2026. If your timeline aligns, a booth conversation can substitute for a written inquiry and lets you bring drawings or a prototype for a face-to-face read. Otherwise, the Contact Us route is the general path.

Practical notes

  • The site shows a "Checkout" link, but no pricing, service rates, or login requirements for project inquiries are described in the available material — do not assume online quoting or self-service onboarding exists.
  • Keep the first message short: stage, device type, target market, and the specific service (development, testing, manufacturing, or a combination). That structure matches how the company describes its own offerings and should route your inquiry faster.