NEN-EN-IEC 61326-2-6
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
inactive
| Organization: | NEN |
| Publication Date: | 1 May 2006 |
| Status: | inactive |
| Page Count: | 37 |
| ICS Code (Electromagnetic compatibility (EMC)): | 33.100 |
| ICS Code (Industrial process measurement and control): | 25.040.40 |
scope:
In addition to the scope of International Standard IEC 61326-1, this part specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.
Document History
June 1, 2021
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
In addition to the scope of IEC 61326-1, this part of IEC 61326 specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for IN VITRO DIAGNOSTIC (IVD) MEDICAL...
June 1, 2013
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
In addition to the scope of IEC 61326-1, this part of IEC 61326 series specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic...
October 1, 2007
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
A description is not available for this item.
NEN-EN-IEC 61326-2-6
May 1, 2006
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
In addition to the scope of International Standard IEC 61326-1, this part specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic...