STN EN IEC 60601-2-75/Zmena A1
Name: | STN EN IEC 60601-2-75/Zmena A1 |
Validity: | Valid |
Number of pages: | 20 |
Language: |
EN
|
Paper: | 14,10€ |
Electronic version |
a) Only read (without ability to print and copy)
12,69€ b) Without ability to print, with ability to copy (printscreen) 14,10€ c) With ability to print and copy (printscreen) 18,33€ |
Slovak title | Zdravotnícke elektrické prístroje. Časť 2-75: Osobitné požiadavky na základnú bezpečnosť a nevyhnutné prevádzkové vlastnosti fotodynamických terapeutických a fotodynamických diagnostických prístrojov |
English title | Medical Electrical Equipment - Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment |
Release Date: | 01. 12. 2024 |
Date of withdrawal: | |
ICS: | 11.040.01 |
Sorting character/National clasification code | 36 4800 |
Level of incorporation: | idt EN IEC 60601-2-75:2019/A1:2024, idt IEC 60601-2-75:2017/AMD1:2023 |
Official Journal | 11/24 |
Amendments | |
Replaced by: | |
Repleces: | |
Note in Official Journal: | STN EN IEC 60601-2-75 z februára 2020 sa bez tejto zmeny A1 môže používať do 31. 7. 2027. |
Subject of the standard: | IEC 60601-2-75:2017 applies to the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment. 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 7.2.13 and 8.4.1 of the general standard. This document applies to photodynamic therapy and photodynamic diagnosis 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 the target area), such equipment also comply with any particular standard specifying safety requirements for the additional function. |
Preview: | Náhľad normy (PDF) |