CEI EN 61010-2-101
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
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| Organization: | CEI |
| Publication Date: | 1 November 2003 |
| Status: | inactive |
| Page Count: | 32 |
scope:
La presente Norma si applica ad apparecchi per scopi medici di diagnosi in vitro (IVD),compresi gli apparecchi medicali di autodiagnosi IVD.
Document History
April 1, 2023
Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
Equipment included in scope
This group safety publication is primarily intended to be used as a product safety standard for the products mentioned in the scope, but shall also be used by technical...
August 1, 2017
Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
IVD medical equipment, whether used alone or in...
CEI EN 61010-2-101
November 1, 2003
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
La presente Norma si applica ad apparecchi per scopi medici di diagnosi in vitro (IVD),compresi gli apparecchi medicali di autodiagnosi IVD.