EN 61010-2-101:2002 (IEC 61010-2-101:2002 (Modified))
Safety requirements for electrical equipment for measurement, control, and laboratory use -- Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
| Status: | Harmonized |
| Poznámka: |
| Full text EAD: | |
| Sector of EN 61010-2-101:2002: | IVDD | In vitro diagnostic medical devices |
| Sphere of EN 61010-2-101:2002: | Regulation No. 22/1997 Sb. - harmonized sphere |
| Publications in the Official Journal: |
(EU)2020/439 (hEN 25. 3. 2020) amendment: (EU)2021/609 (hEN 15. 4.2021) / consolidated text (EU)2020/439 2017/C/389/4 |
| Notified bodies (NANDO): | Notified bodies for Directive EP and Council 98/79/EC |
| ES/EU regulation | ČR regulation | SR regulation |
|---|---|---|
|
Directive EP and Council 98/79/EC
/ will be partial repealed by Regulation (EU)2017/746 of the European Parliament and of the Council (text withamendment (EU)2023/607 / Commission Implementing regulation No (EU)2017/2185 / Commission Decision No 2008/932/ES, 2010/227/EC |
||
| nariadenie vlády SR č. 569/2001 Z.z. (consolidated text) | ||
|
nařízení vlády č. 56/2015 Sb.
repealed by Law No 375/2022 Coll. |
| Released: | December, 2002 |
ČSN
| ČSN EN 61010-2-101:2003 | Note to ČSN EN 61010-2-101:2003: Nahrazena od 24.02.2020 ČSN EN 61010-2-101 ed. 2 (356502) z října 2017 | ||
| Změna Z1-10.17 | Note to Změna Z1-10.17: Nahrazena od 24.02.2020 ČSN EN 61010-2-101 ed. 2 (356502) z října 2017 |
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