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Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators - First Edition; General Instructions No. 1-2

contributor authorCSA - CSA Group
date accessioned2017-09-04T17:52:22Z
date available2017-09-04T17:52:22Z
date copyright1992.08.01 (R 2009)
date issued2009
identifier otherFBWCDFAAAAAAAAAA.pdf
identifier urihttps://yse.yabesh.ir/std/handle/yse/175589
description abstractThis Particular 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).
The following EQUIPMENT is excluded:
- EQUIPMENT intended to be implanted or to be connected to implanted electrodes,
- EQUIPMENT intended for the stimulation of the brain (e.g. electroconvulsive therapy EQUIPMENT),
- EQUIPMENT intended for neurological research,
- cardiac pacemakers,
- body-worn EQUIPMENT,
- STIMULATORS intended for use during surgical procedures,
- EQUIPMENT intended for averaged evoked potential diagnosis,
- EQUIPMENT intended for electromyography,
- EQUIPMENT intended for cardiac defibrillation,
- EQUIPMENT intended only as a transcutaneous nerve and muscle STIMULATOR for pain relief.
languageEnglish
titleCSA CAN/CSA-C22.2 NO. 601.2.10-92num
titleMedical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators - First Edition; General Instructions No. 1-2en
typestandard
page46
statusActive
treeCSA - CSA Group:;2009
contenttypefulltext


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