BS EN IEC 60601-2-37:2024

Medical electrical equipment. Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment | Status: Current

201.1 Scope, object and related standards Clause 1 of IEC 60601‑1:2005 , IEC 60601‑1:2005/AMD1:2012, and IEC 60601‑1:2005/AMD2:2020 applies, except as follows:

201.1.1 *Scope

Replacement: This document applies to the basic safety and essential performance of ULTRASONIC DIAGNOSTIC EQUIPMENT as defined in 201.3.217, hereinafter referred to as me equipment. If a clause or subclause is specifically intended to be applicable to me equipment only, or to me systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to me equipment and to me systems, as relevant. Hazards inherent in the intended physiological function of me equipment or me systems within the scope of this document are not covered by specific requirements in this document except in 201.7.2.13. This document does not cover ultrasonic therapeutic equipment. Equipment used for the imaging or diagnosis of body structures by ultrasound in conjunction with other medical procedures is covered.