CEI EN IEC 61010-2-101:2023
Current
Current
The latest, up-to-date edition.
Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
Available format(s)
Hardcopy , PDF
Language(s)
English
Published date
01-04-2023
Publisher
Important note : Users cannot be edited or removed once added to your Multi user PDF.| Committee |
CT 85/66
|
| DocumentType |
Standard
|
| ISBN |
978-2-8322-6062-3
|
| Pages |
42
|
| PublisherName |
Comitato Elettrotecnico Italiano
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| IEC 61010-2-101:2018 | Identical |
| EN IEC 61010-2-101:2022 | Identical |
| ISO 15223-1:2021 | Medical devices Symbols to be used with information to be supplied by the manufacturer Part 1: General requirements |
| IEC 62366-1:2015 | Medical devices - Part 1: Application of usability engineering to medical devices |
| ISO 13849-2:2012 | Safety of machinery — Safety-related parts of control systems — Part 2: Validation |
| IEC TR 62366-2:2016 | Medical devices - Part 2: Guidance on the application of usability engineering to medical devices |
| IEC 62061:2005+AMD1:2012+AMD2:2015 CSV | Safety of machinery - Functional safety of safety-related electrical, electronic and programmable electronic control systems |
| ASTM D 4169 : 2009 | Standard Practice for Performance Testing of Shipping Containers and Systems |
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