Medovate Limited

Medical device design, contract manufacturing & High and low volume manufacturing

Introduction
Established in 1972, Medovate (Formerly JEB Technologies) brings almost 55 years of engineering expertise to the design and manufacture of medical devices and precision components. We support OEMs at every stage of the product lifecycle, from early-stage development through to validated, high-volume production. Every stage is delivered under one quality system and one roof.

Design and development
For customers developing a new device, our engineering team provides design, prototyping and design-for-manufacture expertise from the earliest stage. Early involvement allows us to optimise part design, tooling strategy and assembly processes before costs are committed. This shortens development timelines and reduces the total cost of manufacture.

Manufacture to specification
For customers with an established design, we manufacture to your drawings and specifications with full traceability and process control. We support technology transfer, first-article inspection and process validation, and scale from low-volume runs to high-volume production. Where appropriate, we offer design-for-manufacture reviews to identify cost and quality improvements.

In-house capabilities

• Tool and jig design and manufacture for metal and plastic components
• A wide variety of injection moulding, including multi-impression, hot runner, insert and over moulding
• 5-axis CNC milling, multi-spindle turning, stamping and forming
• Ultrasonic welding, laser welding and laser marking
• Electronic assembly, passivation and electropolishing
• ISO Class 8 cleanroom facilities
• Complex multi-component assembly

Quality and regulatory
Medovate is certified to ISO 13485:2016. Our in-house quality and regulatory team supports process validation and the critical control systems the medical sector demands. As the legal manufacturer of our own CE-marked medical devices, we bring first-hand regulatory understanding to every customer programme.

Contact us to discuss your project requirements.

JEB are ISO 9001 and 13485 approved and the regulatory and quality control personnel are well versed in the critical control systems required for the medical manufacturing industry. The quality management and regulatory compliance team ensure that products are designed, tested and developed in compliance with regulations and support the validation of manufacturing processes.