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BSI - BS EN IEC 61010-2-091 + A11

Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-091: Particular requirements for cabinet x-ray systems

active, Most Current
Organization: BSI
Publication Date: 31 May 2021
Status: active
Page Count: 38
ICS Code (Electrical and electronic testing): 19.080
ICS Code (Chemical laboratories. Laboratory equipment): 71.040.10
ICS Code (Sterilization and disinfection): 11.080

Document History

BS EN IEC 61010-2-091 + A11
May 31, 2021
Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-091: Particular requirements for cabinet x-ray systems
A description is not available for this item.
BS EN 61010-2-091
August 31, 2012
Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-091: Particular requirements for cabinet x-ray systems
A description is not available for this item.
BS EN 61010-2-091
August 31, 2012
Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-091: Particular requirements for cabinet x-ray systems
A description is not available for this item.

References

This document references:
EN IEC 62061 - Safety of machinery - Functional safety of safety-related control systems
Published by CENELEC on July 1, 2021
This International Standard specifies requirements and makes recommendations for the design, integration and validation of safety-related control systems (SCS) for machines. It is applicable to...
This document references:
EN 60601-1-3 - Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment
Published by CENELEC on April 1, 2008
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document references:
IEC 62304 - Medical device software – Software life cycle processes
Published by IEC on June 1, 2015
Purpose This standard defines the life cycle requirements for MEDICAL DEVICE SOFTWARE. The set of PROCESSES, ACTIVITIES, and TASKS described in this standard establishes a common framework for...
This document references:
IEC 60601-1-3 - Medical electrical equipment – Part 1-3: General requirements for basic safety and essential performance – Collateral Standard: Radiation protection in diagnostic X-ray equipment
Published by IEC on January 1, 2021
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document references:
IEC 60846-1 - Radiation protection instrumentation – Ambient and/or directional dose equivalent (rate) meters and/or monitors for beta, X and gamma radiation – Part 1: Portable workplace and environmental meters and monitors
Published by IEC on April 1, 2009
A description is not available for this item.
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