EVS-EN IEC 80601-2-26:2020

Elektrilised meditsiiniseadmed. Osa 2-26: Erinõuded elektroentsefalograafide esmasele ohutusele ja olulistele toimimisnäitajatele

Kehtiv alates 15.04.2020
IEC 80601-2-26:2019; EN IEC 80601-2-26:2020
Direktiivid või määrused
Standardi ajalugu
IEC 80601-2-26:2019 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROENCEPHALOGRAPHS as defined in 201.3.204, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. This document is applicable to ELECTROENCEPHALOGRAPHS intended for use in professional healthcare facilities, the EMERGENCY MEDICAL SERVICES ENVIRONMENT or the HOME HEALTHCARE ENVIRONMENT. This document does not cover requirements for other equipment used in electroencephalography such as: – phono-photic stimulators; – EEG data storage and retrieval; – ME EQUIPMENT particularly intended for monitoring during electro-convulsive therapy. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title or 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 follows. The clause or subclause applies to ME EQUIPMENT, as default. For ME EQUIPMENT with the corresponding safety measure or function not completely integrated into the ME EQUIPMENT but instead implemented in an ME SYSTEM, the ME EQUIPMENT MANUFACTURER specifies in the ACCOMPANYING DOCUMENTS which functionality and safety requirements are provided by the ME SYSTEM to comply with this document. The ME SYSTEM is verified accordingly. 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. IEC 80601-2-26:2019 cancels and replaces the third edition of IEC 60601-2-26 published in 2012. This edition constitutes a technical revision to align with Amendment 1:2012 of IEC 60601-1:2005, new versions of collateral standards and amendments thereto
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EVS-EN IEC 62368-1:2020+A11:2020

Audio-, video-, informatsiooni- ja sidetehnoloogia seadmed. Osa 1: Ohutusnõuded
Uusim versioon Kehtiv alates 15.04.2020

EVS-EN ISO 80601-2-56:2017/A1:2020

Elektrilised meditsiiniseadmed. Osa 2-56: Erinõuded kehatemperatuuri mõõtmise kliiniliste termomeetrite esmasele ohutusele ja olulistele toimimisnäitajatele
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EVS-EN IEC 61010-2-081:2020

Ohutusnõuded elektrilistele mõõtmis-, juhtimis- ja laboratooriumiseadmetele. Osa 2-081: Erinõuded automaatsetele ja poolautomaatsetele analüüsi- ja muuotstarbelistele laboratooriumiseadmetele
Uusim versioon Kehtiv alates 02.06.2020

EVS-EN IEC 61010-2-010:2020

Ohutusnõuded elektrilistele mõõtmis-, juhtimis- ja laboratooriumiseadmetele. Osa 2-010: Erinõuded laboratoorsetele materjalide kuumutamise seadmetele
Uusim versioon Kehtiv alates 02.06.2020