Therapy equipment

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JS IEC 60601-2-5:2012 Medical electrical equipment Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment

This 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. (Published Document (JS))

JS IEC 60601-2-3:2012 Medical electrical equipment Part 2-3: Particular requirements for the safety of short-wave therapy equipment

This Particular Standard specifies the requirements for the safety of SHORT-WAVE THERAPY EQUIPMENT as defined in Sub-clause 2.1, hereinafter referred to as EQUIPMENT having a RATED OUTPUT POWER not exceeding 500 W. EQUIPMENT having a RATED OUTPUT POWER not exceeding 10 W is exempted from certain requirements of this Standard. Such EQUIPMENT is called low power EQUIPMENT. (Published Document (JS))

JS IEC 60601-2-57:2012 Medical electrical equipment Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use

This Standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of equipment incorporating one or more sources of OPTICAL RADIATION in the wavelength range 200 nm to 3 000 nm, with the exception of laser radiation, and intended to create non-visual photo-biological effects in humans or animals for therapeutic, diagnostic, monitoring, cosmetic/aesthetic or veterinary applications; (Published Document (JS))

JS IEC 60601-2-22:2012 Medical electrical equipment Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment

This Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or animals, classified as a CLASS 3B or CLASS 4 LASER PRODUCT as defined by 3.22 and 3.23 in IEC 60825-1, hereafter referred to as LASER EQUIPMENT. (Published Document (JS))

JS IEC 60601-2-17:2012 Medical electrical equipment Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment

This Particular Standard specifies requirements for the safety of automatically-controlled EQUIPMENT for BRACHYTHERAPY of patients using AFTERLOADING techniques. This Standard specifies requirements for automatically-controlled AFTERLOADING EQUIPMENT (Published Document (JS))

JS IEC 60601-2-6:2012 Medical electrical equipment Part 2-6: Particular requirements for the safety of microwave therapy equipment

This Particular Standard specifies requirements for the safety of MICROWAVE THERAPY EQUIPMENT used in medical practice, as defined in Sub-clause 2.1.101, hereinafter referred to as EQUIPMENT. This standard does not apply to EQUIPMENT specified for hyperthermia. (Published Document (JS))

JS IEC 60601-2-10:2012 Medical electrical equipment Part 2-10: Particular requirements for the safety of nerve and muscle stimulators

This Standard specifies the requirements for the safety of NERVE AND MUSCLE STIMULATORS, as defined in Sub-clause 2.1.101, for use in the practice of physical medicine, hereinafter referred to as STIMULATOR(S). (Published Document (JS))

JS IEC 60601-2-11:2012 Medical electrical equipment Part 2-11: Particular requirements for the safety of gamma beam therapy equipment

This Standard specifies requirements for the safety of GAMMA BEAM THERAPY EQUIPMENT intended for RADIOTHERAPY in human medical practice and includes EQUIPMENT in which the selection and DISPLAY of operating parameters can be controlled by a PROGRAMMABLE ELECTRONIC SYSTEM (PES). (Published Document (JS))

JS IEC 60601-2-29:2012 Medical electrical equipment Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators

This Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of RADIOTHERAPY SIMULATORS, hereafter 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 (Published Document (JS))

JS IEC 60601-2-50:2012 Medical electrical equipment Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment

This Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT PHOTOTHERAPY EQUIPMENT, as defined in 201.3.203 of this standard, also 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. (Published Document (JS))

JS IEC 60601-2-1:2012 Medical electrical equipment Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTRON ACCELERATORS, hereafter referred to as ME EQUIPMENT, in the range 1 MeV to 50 MeV, used for treatment of PATIENTS. This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the manufacture and some installation aspects of ELECTRON ACCELERATORS (Published Document (JS))