Medical Device Drop Testing in Action

Technician operating a custom aluminum-framed drop test rig with a white platform and green background wall.
Resources

Medical Device Drop Testing in Action

YouTube video thumbnail

Medical device drop testing helps ensure that products and packaging survive real-world handling. We demonstrate in-house drop testing on an actual device and its packaging using a custom-built drop tester.

From IEC Standards to Real-World Drops

While passing a standard test like IEC 60601-1 is a good first step, drop testing must also reflect real-world use. Devices get dropped repeatedly, often in uncontrolled settings. Packaging must protect the product all the way from warehouse to end user.

This episode shows how in-house testing setups let engineers explore failure modes before third-party verification. The drop tester featured includes adjustable doors, corner and edge supports, and surfaces for both hardwood and concrete impacts.

Testing Devices and Packaging

During testing, the team drops a medical device on various faces, edges, and corners. The results? Deformation, loose components, and internal rattling—clear signs of structural stress. Eventually, the device fails when dropped on its edge, offering valuable insights for redesign.

Next, they drop test a device package. Each face, edge, and corner is tested—including a downsized box for corner drop demos. A worst-case drop from double height shows whether the packaging holds up under extreme conditions.

Why In-House Drop Testing Matters

Medical device drop testing not only prepares teams for formal third-party tests but also helps identify weaknesses early. It saves time, protects users, and strengthens the final product. And yes—sometimes, it’s just fun to break things on purpose.

Medical Device Design Simulation

We examine when computational modelling and simulation, or CM&S, genuinely supports medical device simulation strategy and when it becomes a costly detour.

Transparent medical device prototype surrounded by computational simulation mesh representing modeling and simulation during medical device development.

Many teams still underuse CM&S, often bringing it late in device validation, when key decisions have already been made. That approach leaves much of the value of CM&S untapped.

Biomedical engineer reviewing a thermal simulation of human head tissue on a monitor, color-mapped from warm to cool gradients

This article traces the Pennes bioheat equation from its 1948 origins to modern multiscale approaches, explaining how engineers select the right level of modelling complexity across device categories.