Medical device manufacturers face a unique challenge when producing consumables such as diagnostic cartridges, IV catheters, and surgical components. These assemblies often fall into the “low mix, high volume” category or limited product variation but massive daily output. Meeting that demand with manual processes stretches labor, risks quality, and drives up costs, especially under strict regulatory oversight. Automation provides the consistency and throughput these assemblies require.
Unlike high mix, low volume operations, which require rapid changeovers (flexible feeders, for example), low mix, high volume lines are ideal for dedicated automation. Once the equipment is dialed in, every cycle repeats with precision. Automation not only stabilizes output but also frees engineering teams from constant oversight of operator performance. In regulated environments, that consistency translates directly to reduced compliance risk.
Together, these layers create a repeatable workflow where every part is built and verified to specification.
Most automated equipment isn’t built piece by piece on the production floor. It’s engineered and tested as a complete line in advance. After passing factory acceptance testing, the system is shipped in and set up to run as a self-contained unit. This way, production teams don’t lose weeks trying to stitch automation into a manual process. Instead, they bring the line online quickly and start seeing output improve almost immediately.
For medical assemblies, speed alone is not enough. Automation must maintain cleanliness, accuracy, and traceability to satisfy regulatory standards. Every inspection camera, sensor, and test station contributes to a closed-loop system that documents compliance while maximizing throughput. The result is a line that can run continuously with fewer operators, lower training costs, and a more consistent product output.
Contact Intec Automation today to discuss how purpose-built equipment can streamline your low mix, high volume medical assemblies.