IEC 60601-1-11 Medical Electrical Equipment, Part 1-11: Medical Electrical Equipment and Medical Electrical Systems Used in the Home Health Care Environment

Medical Device Tests

IEC 60601-1-11 Medical Electrical Equipment, Part 1-11: Medical Electrical Equipment and Medical Electrical Systems Used in the Home Health Care Environment

EUROLAB laboratory provides testing and compliance service within the scope of IEC 60601-1-11 standard. IEC 60601-1-11 medical device testing evaluates mechanical strength. Specifically, it addresses the ability of medical devices to withstand shipping hazards. It focuses on problems that may occur in the transportation of devices.

IEC 60601-1-11 Medical Electrical Equipment, Part 1-11: Medical Electrical Equipment and Medical Electrical Systems Used in the Home Health Care Environment

The shipping may be from the manufacturer to a distributor, healthcare provider or retailer. Hazards can also occur while having sick devices. It is important that medical device manufacturers complete the required package tests. This will reduce the amount of damage and return that may occur.

Even normal use of medical devices in the home healthcare environment can be dangerous. Patients and their families, especially children, can be rude when using the equipment. To address these conditions, test methods are designed according to medical device usage categories.

The IEC 60601-1-11 test standard assigns categories to devices and these categories are based on whether the equipment is designed to be stationary or transported during normal use.

It should be carried regardless of the end use or location of the medical equipment. As a result, medicinal products will likely be exposed to mechanical stresses. These stresses can include vibrations and shocks caused by bumps and falls. These bumps and falls can be loading and unloading the equipment on transport. It can also be done only by the transportation trip itself.

The IEC 60601-1-11 transit test has two main equipment classifications. The first is the use that cannot be operated in transit. This is equipment that is not expected to be moved during operation. The second classification can be operated in transit. This is the medical device that contains the operation while its intended use is being carried. Examples are wheelchair-bound, body-worn or hand-held devices. Devices used in cars, boats, trains, planes or buses are also considered in this classification.

It should be noted that some equipment may be interchangeable. In some settings, it can not be operated in transit, while in other settings, it can be operated in transit. For example, most body worn equipment is considered operable in transit. However, if the device is for a patient who is in bed, it will be considered that the device cannot be used in transit. Another example is a portable fan. It can be designed for a seated patient (non-transit) or used when mounted in a wheelchair (transit).

EUROLAB assists manufacturers with IEC 60601-1-11 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.

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