STN EN IEC 61010-2-101
Name: | STN EN IEC 61010-2-101 |
Validity: | Valid |
Number of pages: | 24 |
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 | Bezpečnostné požiadavky na elektrické zariadenia na meranie, riadenie a laboratórne použitie. Časť 2-101: Osobitné požiadavky na diagnostické zdravotnícke zariadenia in vitro (IVD) |
English title | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment |
Release Date: | 01. 02. 2023 |
Date of withdrawal: | |
ICS: | 11.040.55, 19.080 |
Sorting character/National clasification code | 36 2000 |
Level of incorporation: | idt IEC 61010-2-101:2018, idt EN IEC 61010-2-101:2022 |
Official Journal | 01/23 |
Amendments | Zmena A11 V 01/23 |
Replaced by: | |
Repleces: | STN EN 61010-2-101:2017-07 (36 2000) |
Note in Official Journal: | |
Subject of the standard: | IEC 61010-2-101:2018 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety publication, as specified in IEC Guide 104. This document has been prepared in close collaboration with Working Group CENELEC BTTF 88.1. This third edition cancels and replaces the second edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition: - adaptation of changes introduced by Amendment 1 of IEC 61010-1; - added tolerance for stability of AC voltage test equipment to Clause 6. This Part 2-101 is intended to be used in conjunction with IEC 61010-1. It was established on the basis of the third edition (2010) and its Amendment 1 (2016). |
Preview: | Náhľad normy (PDF) |