medicalmurray.com

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:

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.

Medical Murray specializes in catheter assembly for vascular, gastrointestinal, urologic, and other interventional markets. The company is a contract development and manufacturing organization (CDMO) for minimally invasive medical devices and implants, and it supports catheter programs from original design and prototyping through testing and commercial manufacturing. This makes it a relevant fit if your project involves a complex catheter for a minimally invasive procedure and you need an external partner for development, assembly, or both.

Catheter Markets Served

Medical Murray's stated catheter focus spans several clinical areas:

The company describes itself as specializing in catheter assembly for these markets rather than offering a single standard product line. If your device falls outside these areas, the broader interventional device and implant capabilities may still apply, but the catheter-specific fit is strongest in the markets above.

Complex Catheters and Catheter Shafts

Two capability areas matter most for catheter projects:

• Complex catheters. Medical Murray lists complex catheters among its core technologies, alongside implants and material technologies. This points to assembly work on catheters that go beyond simple tubing.
• Catheter shafts. Under material technologies, the company states that it produces catheter shafts, along with ePTFE implants and covered stents and frames. Shaft production in-house can matter when a program needs tighter control over the build of the catheter body rather than sourcing shafts separately.

For a project team, the practical question is whether your catheter requires custom shaft construction, multi-component assembly, or both. Medical Murray's listed capabilities cover each of these areas.

Development Through Manufacturing

Catheter assembly is one service within a broader concept-to-commercialization offering. The company lists three main service areas: development, testing, and manufacturing. Within development, its engineering team assists with original designs, problem solving, and custom manufacturing processes, including design, prototyping, and testing.

This structure suits programs that are still defining the device as well as those with a finalized design that need a manufacturing partner. The site describes support "from concept through commercialization," so a catheter project can start at prototyping and continue into production with the same organization.

Quality and Regulatory Credentials

For catheter programs, supplier qualifications are often a gating factor. Medical Murray states that it is:

• FDA Registered
• ISO 13485 Certified
• ISO/IEC 17025:2017 Accredited

These credentials are relevant when evaluating a contract manufacturer for a device that will require regulatory submission. Confirm the scope of each certification against your specific device type and processes during supplier qualification rather than relying on the general listing alone.

How to Decide If It Fits Your Project

Use these conditions to judge fit:

• Strong fit: Your device is a catheter for vascular, gastrointestinal, urologic, or another interventional market, and you need assembly plus development or manufacturing support.
• Possible fit: Your device is an interventional device or implant adjacent to catheters, such as a delivery system, covered stent, or sensor-based implant.
• Check first: Your project requires capabilities not listed on the site, or you need pricing and timeline details. The website does not publish pricing; the only pricing-related link is a checkout page, and no rates or terms are stated. Contact the company directly for quotes and availability.

The site also references events such as MD&M West 2026 (Anaheim, California, Booth #1521, February 3–5, 2026), which can be a low-commitment way to discuss a catheter project in person.

To move forward, the most useful first step is to describe your catheter's clinical market, construction (shaft, components, materials), and current stage (concept, prototype, or design freeze) when contacting Medical Murray, so the response addresses assembly and development needs specifically.

Medical Murray develops and manufactures implants and their delivery systems as part of its contract development and manufacturing (CDMO) services for minimally invasive medical devices. Its stated implant capabilities cover covered stents and frames, bioabsorbables, textiles, and sensors, supported by in-house material technologies such as ePTFE implant production. This makes the company relevant if you need a partner that can take an implant concept through design, prototyping, testing, and manufacturing rather than only supplying one isolated service.

Implant Types and Technologies Covered

Medical Murray's site groups its implant work under three related areas: implants and delivery systems, complex catheters, and material technologies. The implant-specific examples it names are:

• Covered stents and frames — implant structures with covering materials, developed together with their delivery systems.
• Bioabsorbables — implants designed to be absorbed by the body.
• Textiles — textile-based implant components.
• Sensors — sensor elements incorporated into implant or delivery-system designs.
• ePTFE implants — produced through the company's material technologies, alongside ePTFE-covered stents and frames and catheter shafts.

A practical point from the site's structure: implants are presented together with their delivery systems, not as standalone hardware. If your device requires a delivery mechanism (for example, a covered stent that must be compressed, delivered, and deployed), that combined scope is the relevant service area to discuss.

How Implant Work Connects to Testing and Manufacturing

The company describes itself as supporting a device "from concept through commercialization," with development, testing, and manufacturing listed as its core service categories. For an implant program, that means the same organization can potentially cover:

The ISO/IEC 17025 accreditation is specifically a laboratory competence accreditation, which is relevant if your testing needs to be traceable to an accredited lab. The ISO 13485 certification covers medical device quality management systems. Both are stated on the site; confirm the exact scope of each certificate with the company for your device type.

Markets and Device Context

Medical Murray lists the following markets for its interventional devices: aortic, structural heart, neurovascular, cardiovascular, peripheral vascular, orthopedics, gastroenterology, and urology. Implant and delivery-system work sits within this interventional-device focus, so the fit is strongest for minimally invasive implants rather than, say, large orthopedic hardware or active implantable electronics.

When This Is the Right Fit — and What to Verify

Consider Medical Murray for implant work if you need a single partner spanning design, testing, and contract manufacturing, particularly for covered stents, bioabsorbable or textile-based implants, sensor-integrated devices, or ePTFE components.

Before engaging, verify the following directly, since the public site does not detail them:

• Specific implant experience in your clinical area and device class.
• Cleanroom and processing capabilities for your materials (the site does not publish facility or cleanroom specifications).
• Testing scope under the ISO/IEC 17025 accreditation — which test methods are actually covered.
• Commercial terms, timelines, and whether a checkout or online ordering path applies to your engagement (the site links a "Checkout" page, but nothing indicates that development services are transacted online).

The most direct next step is the company's contact channel, described on the site as the way to "get started." You can also review its blog resources on rapid prototyping and verification testing, which reflect its stated approach to building and testing earlier in development.

Medical Murray is a contract development and manufacturing organization (CDMO) focused on minimally invasive medical devices and implants. It supports device work from concept through commercialization, combining design, prototyping, testing, and manufacturing services. It is a relevant partner if you need catheter, implant, or material-technology expertise and want one organization to carry a device from early development into production.

What Medical Murray does

The company describes its role as developing, building, and testing medical devices. Its services are grouped into three areas:

• Development — original designs, problem solving, and custom manufacturing processes, including design and prototyping
• Testing — verification and other testing work as part of device development
• Manufacturing — contract manufacturing of interventional devices and implants

The stated approach is collaborative, with the company positioning itself as a partner for engineering, manufacturing, and quality services rather than only a production vendor.

Core technology areas

Complex catheters

Medical Murray specializes in catheter assembly for vascular, gastrointestinal, urologic, and other interventional markets. This is the area to look at if your device involves multi-component catheter construction rather than a simple extruded tube.

Implants and delivery systems

The company develops and manufactures implants together with their delivery systems. Named examples include covered stents and frames, bioabsorbables, textiles, and sensors. Working on the implant and its delivery system together matters when deployment behavior and implant design are tightly coupled.

Material technologies

This covers production of ePTFE implants, covered stents and frames, and catheter shafts. Material choice and processing often determine device performance, so this capability is relevant when your design depends on a specific material rather than a standard component.

Markets served

Medical Murray lists experience across these device markets:

If your device falls in one of these areas, the company's existing process and material experience may shorten the learning curve. If it falls outside them, ask specifically how your device type maps to their capabilities before assuming a fit.

Quality and regulatory credentials

The site states the company is:

• FDA Registered
• ISO 13485 Certified
• ISO/IEC 17025:2017 Accredited

These are the credentials to verify early in a partner evaluation, since they affect whether a supplier can support your regulatory pathway. Confirm the scope of each certification against your specific device and processes rather than relying on the headline claims.

When Medical Murray is a good fit

Consider Medical Murray when:

• Your device is a minimally invasive device, catheter, or implant in one of the listed markets
• You need development and manufacturing under one organization, from concept to commercialization
• Your design depends on catheter assembly, implant delivery systems, or materials such as ePTFE
• You want a partner with documented quality system certifications

Look elsewhere, or ask more detailed questions first, if your device is outside the listed technology and market areas, or if you need a capability the company does not describe on its site.

How to evaluate fit

1. Define your device and stage. Write down the device type, target market, and whether you need design, testing, manufacturing, or all three.
2. Map it to the core technologies. Check whether your work involves complex catheters, implants and delivery systems, or material technologies like ePTFE.
3. Check the market list. Confirm your target market appears among those the company names.
4. Verify credentials for your pathway. Ask for the scope of the ISO 13485 and ISO/IEC 17025 accreditations relative to your device and test methods.
5. Contact the company. The site directs prospective partners to contact Medical Murray to get started; use that first conversation to confirm capabilities, capacity, and timeline for your specific project.

The main pitfall is treating a broad service list as proof of fit for any device. Match your specific technology, market, and regulatory needs to the company's stated capabilities before committing to a development or manufacturing engagement.

Medical Murray holds three credentials listed on its website: it is FDA Registered, ISO 13485 Certified, and ISO/IEC 17025:2017 Accredited. Together these cover the three things a buyer typically checks before qualifying a contract development and manufacturing organization (CDMO): a regulatory footprint with the FDA, a certified quality management system, and accredited testing capability. The company describes itself as a trusted partner for engineering, manufacturing, and quality services.

The Three Credentials and What Each One Signals

A practical reading: ISO 13485 addresses how the organization manages quality across its processes, while ISO/IEC 17025 accreditation is specific to laboratory testing and calibration. For a project where verification testing is part of the scope, the second credential is the one to look at closely.

Where These Fit in Medical Murray's Service Model

Medical Murray is a contract development and manufacturing organization for minimally invasive medical devices and implants, supporting a device from concept through commercialization. Its listed services are development, testing, and manufacturing, with core technology areas in complex catheters, implants, and material technologies.

That scope explains why the credential set is structured the way it is:

• Development and manufacturing map to the ISO 13485 quality system and FDA establishment registration.
• Testing maps to the ISO/IEC 17025:2017 accreditation, which is the credential tied specifically to laboratory work.
• Markets served include aortic, structural heart, neurovascular, cardiovascular, peripheral vascular, orthopedics, gastroenterology, and urology — so the quality expectations you bring should match the risk profile of your device, not just the supplier's general certification list.

The company's own resources reflect this emphasis. A blog post on verification testing describes treating verification as an end-of-project step as "one of the biggest mistakes" in device development, and a separate post argues for prototyping early to learn faster. Both point to testing and iteration being positioned as front-loaded activities rather than a final checkbox.

How to Verify Before You Qualify the Supplier

Certifications are claims until you confirm them. A workable sequence:

1. Ask for current certificate copies. Request the ISO 13485 certificate and the ISO/IEC 17025:2017 accreditation, and check the certificate holder name, scope, and expiry date against your project.
2. Confirm the scope covers your work. A certificate can be valid but narrow — verify that the activities you need (for example, catheter assembly or implant manufacturing) fall inside the stated scope.
3. Check the FDA registration status. Ask for the establishment registration details and confirm they match the site that will actually do your work.
4. Match credentials to your device class and market. If you are commercializing outside the U.S., ask what other registrations or audit history apply to your target markets; the website lists only the three credentials above.
5. Request the testing accreditation schedule. For ISO/IEC 17025, ask which tests are within the accredited scope, since accreditation applies to specific methods rather than to a lab as a whole.

Expected result: you end up with a documented, scope-matched credential file rather than a general assurance that the supplier is "certified."

Common Sticking Points

• Registration is not approval. FDA registration means the establishment is registered; it does not mean a particular device is cleared or approved. Keep those separate in your supplier records.
• Certification is not project-specific. ISO 13485 certification covers the quality system, not your device's design outputs. Your own design controls and verification activities still apply.
• Accreditation scope matters. ISO/IEC 17025 accreditation is granted for defined tests; confirm the specific methods your verification plan depends on are included.
• Certificates expire. Build a renewal check into your approved-supplier list so an expired certificate does not surface during an audit.

If your decision hinges on testing independence or on regulatory coverage beyond the U.S., those are the two areas to raise directly with Medical Murray before qualification — the public site confirms the three credentials but does not detail scope, certificate dates, or additional market registrations.