Download white papers from Lowell to learn how different processes and methods can improve your medical device manufacturing outcomes.
Realizing our customers’ design intent is one of our goals with any project. To share more about how a design intent strategy can improve the product development process, we created the white paper, “Improve Device Development with a Clear Design Intent Strategy.” Download the white paper now to learn more about what’s included in design intent discussions, and how GD&T paired with 3D solid models can clarify design intent and improve device development.
Metrology matching, also called inspection matching, is a leading way to solve this issue. The process aligns two separate inspection systems, one from the OEM and one from the supplier. This ensures that everyone is on the same page for inspection and measurement, even if they use different equipment and measurement methods.
Critical feature confirmation (CFC) helps design teams determine which medical device features are critical so they can streamline the design, review and quality control processes. Download this white paper to learn more about this process and how it can help you improve design and testing of a new medical device.
Ensuring your engineering, manufacturing, and quality teams are aligned is critical to successful medical device development. Then why are there still so many issues with design intent not matching the parts created? Learn more about critical steps in the GD&T process and ASME Y14.5M 2009 standards to improve your outcomes.
Precision geometrical dimensioning and tolerancing (GD&T) and profile tolerancing are key design methods to accelerate a medical device’s time to market by reducing inspection time. This white paper explores the positive impact that these methods has on three types of inspection: setup, in-process and final.
This white paper about statistical methods in precision machining offers an overview of how to use data to reduce critical features, create a design of experiments and how to recognize if your current supplier has the equipment and skill sets to fully utilize manufacturing data to advance your projects.
If the tolerance stackup is done correctly, all medical device components will assemble together and function as intended. This white paper explores the benefits and limitations of three common methods for analyzing and presenting tolerance stackups in multicomponent medical device assemblies.
This white paper offers an overview of profile tolerancing, geometrical dimensioning and tolerancing (GD&T), and profile analysis software, as well as the benefits and limitations of a profile tolerancing approach for device design and manufacturing.
Lowell automated its inspection equipment to take advantage of greater cost savings and higher production rates, and allow its highly trained team to focus on higher-level tasks. Read this white paper to learn about how we evaluated our processes, chose the right equipment and realized a number of benefits through automation.