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In some instances, medical equipment may be used to treat. However, they could cause serious adverse side effects. In this situation, the use of the equipment is obligatory for decreasing the possibility of occurring negative effects. One of the documents that specifies such a case is EN 60601-2-11:2015. This document is about the safety and performance of gamma-beam therapy equipment, and also multi-source stereotactic radiotherapy equipment. The 60601 standard in question is part of that series. It defines the standards that manufacturers must adhere to when developing and fabricating the gamma beam therapy equipment. It sets limits on tolerance to make sure that no interlocks will be used to interrupt, stop or stop irradiation that exceeds the limits. For each requirement there are particular requirements for type tests and site tests. Click here to find out more about our requirements for manufacturers whose firms are connected with gamma-beam therapy equipment. Have a look at the top cen catalog standards en-14803-2020 blog.

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