60601-1 General Standard plus particular standards
- the company I work for creates an x-ray component integrated into a larger medical device. 60601-2-44 applies to our component but other particular standards apply to other components within the medical device, and being created by another company. Has any one found conflicting requirements between the standards? and if so, how is the dominant standard/requirement determined? Is there a hard and fast rule or is it simply risk based decision making?