MedRes - Medical Research Engineering
Csongvay Péter is a Junior R&D Engineer at MedRes - Medical Research Engineering since February 2022, engaged in the feasibility study of a novel cardioscope system for a US customer. Key responsibilities include designing and testing prototypes, managing suppliers, and organizing cadaver studies. Csongvay previously participated in a short-term assignment providing engineering support for the development of a hysteroscope. Prior experience includes serving as an R&D Engineering Trainee at Sanatmetal Ltd., focusing on a porous Titanium spine implant and a new fixation system, a Research Assistant at the Gwangju Institute of Science and Technology exploring polymer-based 3D printing for EEG applications, and an intern at PaB Kereskedelmi és Szolgáltató Kft. Csongvay holds a Master's and a Bachelor's degree in Mechanical Engineering from Budapest University of Technology and Economics, along with a high school diploma in Mathematics and Computer Science from Bolyai Farkas Teoretic High School.
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MedRes - Medical Research Engineering
MedRes is a medical technology company with 20 years of experience in designing, developing, and manufacturing medical devices. We specialize in complex surgical systems, including minimally invasive handheld devices, fluid management systems, controllers and the software that controls their various functions. We offer a range of services to clients of all sizes including contract manufacturing, contract development, supply chain management, and consulting services in quality assurance, regulatory and clinical affairs. We have extensive experience in various medical specialties like gynecology, urology, cardiology, airway management, gastroenterology, and orthopedics, allowing us to handle their unique challenges and opportunities. We provide high-quality, customized manufacturing solutions for small to high volume production, from component manufacturing to the assembly of finished medical devices. Our production facility includes a Class 8 cleanroom and controlled manufacturing areas. We offer contract development services personalized for each project to guide you through all stages of medical device development. They include ideation, designing, prototyping, testing and transfer to pilot and volume manufacturing. Ensuring quality is our top priority, and our development and manufacturing processes strictly adhere to industry standards such as ISO 13485 and FDA regulations. Our QA team has deep experience in quality system development, design control processes, and regulatory requirements for market approval in the US and EU, with strong connections to clinical and academic centers. We take pride in our multiple medical devices that are currently on the market, and we are proud that many of our successful projects have been integrated into major medical device company portfolios and have gained worldwide recognition.