CSA CAN/CSA-C22.2 NO. 60601-2-5:11 Medical electrical equipment - Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment - Third Edition
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- ISO 18405 Underwater acoustics - Terminology - First Edition
- 01
- ISO 18405 Underwater acoustics - Terminology - First Edition
- 01.040
- ISO 18405 Underwater acoustics - Terminology - First Edition
- 01.040.17
- 17
- ISO 18405 Underwater acoustics - Terminology - First Edition
- 17.140
- ISO 18406 Underwater acoustics - Measurement of radiated underwater sound from percussive pile driving - First Edition
- IEC 60500 Underwater acoustics - Hydrophones - Properties of hydrophones in the frequency range 1 Hz to 500 kHz - Edition 2.0
- ISO ISO/IEC GUIDE 98 Guide to the expression of uncertainty in measurement (GUM) - Edition 1; ***IMAGE NOT AVAILABLE AT IHS***
- Картотека зарубежных и международных стандартов
CSA Standards
Medical electrical equipment - Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment - Third Edition
N CAN/CSA-C22.2 NO. 60601-2-5:11
Annotation
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ULTRASONIC PHYSIOTHERAPY EQUIPMENT as defined in 201.3.216, hereafter referred to as ME EQUIPMENT.
This standard only relates to ULTRASONIC PHYSIOTHERAPY EQUIPMENT employing a single plane unfocused circular transducer per TREATMENT HEAD, producing static beams perpendicular to the face of the TREATMENT HEAD.
This standard can also be applied to ULTRASONIC PHYSIOTHERAPY EQUIPMENT used for compensation or alleviation of disease, injury or disability.
In the case of combined EQUIPMENT (e.g. EQUIPMENT additionally provided with a function or an APPLIED PART for electrical stimulation) such EQUIPMENT shall also comply with any particular standard specifying safety requirements for the additional function.
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 standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.
NOTE 1 See also 4.2 of the general standard.
This particular standard does not apply to:



