iTeh Standards logo
EURUSD
Your shopping cart is empty.
IEC

JWG 6 - TC 62/SC 62D/JWG 6

TC 62/SC 62D/JWG 6

General Information

Status
Active
Work Field
Information technology
Parent
SC 62D - Particular medical equipment, software, and systems

Frequently Asked Questions

JWG 6 is a Technical Committee within the International Electrotechnical Commission (IEC). It is named "TC 62/SC 62D/JWG 6". This committee has published 6 standards.

JWG 6 develops IEC standards in the area of Information technology. Currently, there are 6 published standards from this technical committee.

The International Electrotechnical Commission (IEC) is the world's leading organization for the preparation and publication of international standards for electrical, electronic, and related technologies. Founded in 1906, the IEC provides a global platform for companies, industries, and governments to meet, discuss, and develop the international standards they require.

A Technical Committee (TC) in IEC is a group of experts responsible for developing international standards in a specific technical area. TCs are composed of national member body delegates and work through consensus to create standards that meet global industry needs. Each TC may have subcommittees (SCs) and working groups (WGs) for specialized topics.

Standardization Organization
ICS
Directive
Mandate
50
IEC
ISO 80601-2-55:2018/AMD1:2023(Amendment)
Amendment 1 - Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors
  • Standard
    8 pages
    English language
    sale 15% off
  • Standard
    8 pages
    French language
    sale 15% off
IEC
ISO 80601-2-55:2018(Main)
Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors

ISO 80601-2-55:2018 specifies particular requirements for the basic safety and essential performance of a respiratory gas monitor (rgm), hereafter referred to as me equipment, intended for continuous operation for use with a patient.
ISO 80601-2-55:2018 specifies requirements for
- anaesthetic gas monitoring,
- carbon dioxide monitoring, and
- oxygen monitoring.
NOTE 1 An rgm can be either stand-alone me equipment or integrated into other equipment, e.g. an anaesthetic workstation or a ventilator.
ISO 80601-2-55:2018 is not applicable to an rgm intended for use with flammable anaesthetic agents.
If a clause or subclause is specifically intended to be applicable to me equipment only or to me systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to me equipment and to me systems, as relevant.
Hazards inherent in the intended physiological function of me equipment or me systems within the scope of this document are not covered by specific requirements in this document except in IEC 60601‑1:2005+Amd 1:2012, 7.2.13 and 8.4.1.
NOTE 2 Additional information can be found in IEC 60601‑1:2005+Amd 1:2012, 4.2.

  • Standard
    59 pages
    English language
    sale 15% off
  • Standard
    59 pages
    French language
    sale 15% off
IEC
ISO 80601-2-55:2011(Main)
Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors

ISO 80601-2-55:2011 specifies particular requirements for the basic safety and essential performance of a respiratory gas monitor (RGM) intended for continuous operation for use with a patient. ISO 80601-2-55:2011 specifies requirements for: - anaesthetic gas monitoring, - carbon dioxide monitoring, and - oxygen monitoring. ISO 80601-2-55:2011 is not applicable to an RGM intended for use with flammable anaesthetic agents.

  • Standard
    52 pages
    English language
    sale 15% off
  • Standard
    52 pages
    French language
    sale 15% off
50