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Medical Murray will conduct web based patent searches and can provide engineering” opinions concerning your device. Please note that these opinions carry no legal weight. In addition, we will provide engineering descriptions, drawings, etc. to support the writing of your patent by a qualified patent attorney. We suggest you engage the services of a patent attorney experienced with medical devices in order to conduct a complete patent search. We have a local medical device patent attorney firm we can refer you to if desired.
Medical Murray uses brainstorming sessions to identify new concepts or methods of meeting the customer’s requirements. These are consolidated, rated for their effectiveness and reviewed with the customer for further evolution.
Our team of biomedical, mechanical and industrial design engineers deliver creative medical device design services, using a combination of a quality education, varied device development experience, and state of the art software tools.
Rapid prototyping and testing of devices is critical to the development process. Medical Murray maintains an extensive inventory of materials and equipment to rapidly produce very complex devices ranging from multilumen composite catheters to overmolded titanium inserts for implants.
Medical Murray possesses equipment for measuring strength, elongation, dimensions, pressures, kinking and catheter motion. The standard equipment is regularly calibrated by our quality department. In addition, we build specialized testing equipment that is product specific such as particulate contamination, fatigue, creep, flow rate, needle puncture, etc. In addition we can arrange for animal studies.
We are experienced in submitting 510(k) documentation for FDA approval on behalf of our customer. Data supporting PMA, IDE and CE marking are readily available from our development documentation. Medical Murray has the experience you need to support you in determining the FDA approval route.
Devices for use in regulatory testing, animal studies, clinical trials and first production runs can be produced in one of our pilot production controlled environment rooms. We maintain our 1000 square foot cleanrooms at an ISO class 7. When the device is ready for full production, the product line can be transferred to our manufacturing facility or transferred to your designated manufacturer.
Everything we create for you during your project is yours, to take with you at anytime, or to be transferred to the manufacturer of your choice.
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