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BSI - BS EN ISO 5360 - TC

Tracked Changes (Redline) - Anaesthetic vaporizers - Agent-specific filling systems

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Organization: BSI
Publication Date: 26 February 2020
Status: active
Page Count: 62
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

BS EN ISO 5360 - TC
February 26, 2020
Tracked Changes (Redline) - Anaesthetic vaporizers - Agent-specific filling systems
A description is not available for this item.

References

This document references:
ISO 1101 - Geometrical product specifications (GPS) - Geometrical tolerancing - Tolerances of form, orientation, location and run-out
Published by ISO on February 1, 2017
This document defines the symbol language for geometrical specification of workpieces and the rules for its interpretation. It provides the foundation for geometrical specification. The illustrations...
This document references:
DIN 6164-2 - DIN colour chart; specification of colour samples
Published by DIN on February 1, 1980
A description is not available for this item.
This document references:
EN 15986 - Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates
Published by CEN on March 1, 2011
This European Standard specifies requirements for the labelling of a medical device or parts of a medical device to indicate the presence of phthalates, when required by Annex I of Directive...
This document references:
BS 5252 - Framework for Colour Co-Ordination for Building Purposes
Published by BSI on June 30, 1976
Comprises folder containing a colour chart consisting of 237 colours, a chart showing their approximate Munsell references and text which includes explanations of the visual attributes, hue,...
This document references:
EN 15986 - Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates
Published by CEN on March 1, 2011
This European Standard specifies requirements for the labelling of a medical device or parts of a medical device to indicate the presence of phthalates, when required by Annex I of Directive...
This document references:
IEC 62366-1 - Medical devices – Part 1: Application of usability engineering to medical devices
Published by IEC on June 1, 2020
This part of IEC 62366 specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY of a MEDICAL DEVICE as it relates to SAFETY. This USABILITY ENGINEERING (HUMAN...
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