Medical Murray Designs, Develops and Manufactures Your Medical Devices
As Medical Murray produces no products of their own, we can focus 100% on the design, development and production of our customer's medical devices.
Design, development, testing, validation and sourcing of market-appropriate packaging and package testing processes and protocols.
We will manage and support the development of appropriate biocompatibility protocols and testing required by the FDA.
Medical Murray will manage all aspects of the sterilization process including:
We are ISO 13485 certified for both design and manufacturing. We are FDA registered.
Whether you need to produce 1 or a few hundred thousand pieces for demonstrations, handouts, prototypes, clinical trials, early stage production, or mass production, in addition to designing and developing your device, we will manufacture or take responsibility for manufacturing your medical device.
Production Services Include:
- Cleanroom manufacturing and assembly of your device
- Perform required testing
- Apply finished device packaging
- Manage the sterilization process and lot release testing
Examples of devices we have manufactured for customers:
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Assembly Capabilities
- Part design for all medical materials
- Thermoplastic and thermoset injection molding
- Assembly of all medical materials
- Catheter component and system design and assembly
- Shaped memory materials (Nitinol) forming and assembly
- Catheter tip molding
- Silicone molding and forming processes
- Braiding processes and technologies (up to 48 pic count)
- Bonding processes using solvents, adhesives, epoxies, and polymers
- Soldering
- Mechanical, and electro-mechanical assembly
- Functional and performance testing of solids and liquids; auto & manual
- Welding, using thermal, chemical, ultrasonic, and staking processes
- Cleaning using ultrasonic, fluid bed, chemical, and other processes
Packaging
Design, development, testing, validation and sourcing of market-appropriate packaging and package testing processes and protocols.
Biocompatibility
We will manage and support the development of appropriate biocompatibility protocols and testing required by the FDA.
Sterilization
Medical Murray will manage all aspects of the sterilization process including:
- Determination of the best process for your device, based on desired materials
- Validations
- Audits
- Qualifications and re-qualifications
Quality System
We are ISO 13485 certified for both design and manufacturing. We are FDA registered.
Let Us Listen To How We Can Help You With Your Low Volume Production Requirements
Medical Device Design & Development