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BSI - BS 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: BSI
Publication Date: 9 December 2002
Status: inactive
Page Count: 26
ICS Code (Electrical and electronic testing): 19.080
ICS Code (Chemical laboratories. Laboratory equipment): 71.040.10
ICS Code (Diagnostic equipment): 11.040.55

Document History

BS EN 61010-2-101 + A11
April 30, 2023
Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
A description is not available for this item.
BS EN 61010-2-101
March 31, 2017
Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
A description is not available for this item.
BS EN 61010-2-101
December 9, 2002
Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
A description is not available for this item.

References

This document references:
7000 DATABASE SNAPSHOT - Graphical symbols for use on equipment - Registered symbols
Published by ISO on June 3, 2020
A description is not available for this item.
This document references:
IEC 60073 - Basic and Safety Principles for Man-Machine Interface, Marking and Identification - Coding Principles for Indicators and Actuators
Published by IEC on May 1, 2002
This International Standard establishes general rules for assigning particular meanings to certain visual, acoustic and tactile indications in order to – increase the safety of persons, property...
This document references:
EN 60073 - Basic and Safety Principles for Man-Machine Interface, Marking and Identification - Coding Principles for Indication Devices and Actuators
Published by CENELEC on July 1, 2002
A description is not available for this item.
This document references:
EN ISO 14971 - Medical devices - Application of risk management to medical devices
Published by CEN on December 1, 2019
This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process...
This document references:
EN 592 - Instructions for Use in Vitro Diagnostic Instruments for Self-Testing
Published by CEN on February 1, 2002
A description is not available for this item.
This document references:
EN 591 - Instructions for Use for In Vitro Diagnostic Instruments for Professional Use
Published by CEN on March 1, 2001
A description is not available for this item.
This document references:
DS/ISO/IEC GUIDE 51 - Safety aspects - Guidelines for their inclusion in standards
Published by DS on April 7, 2014
ISO/IEC Guide 51:2014 provides requirements and recommendations for the drafters of standards for the inclusion of safety aspects in standards. ISO/IEC Guide 51:2014 is applicable to any safety...
This document references:
BS EN ISO 14971 + A11 - Medical devices - Application of risk management to medical devices
Published by BSI on December 31, 2019
A description is not available for this item.
This document references:
D4169 - Standard Practice for Performance Testing of Shipping Containers and Systems
January 1, 2022
This practice provides a uniform basis of evaluating, in a laboratory, the ability of shipping units to withstand the distribution environment. This is accomplished by subjecting them to a test plan...
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