Medical electrical equipment - Part 2-84: Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment

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CSA Group
Standards Development Organisation:
Working Program:
Designation Number:
CSA C22.2 No. 80601-2-84
Standard Type:
National Standard of Canada - Adoption of International Standard
Standard Development Activity:
New Edition
ICS code(s):
11.040.10
Status:
Proceeding to development
SDO Comment Period Start Date:
SDO Comment Period End Date:
Posted On:

Scope:

Scope

Replacement: 

NOTE 1 There is guidance or rationale for this subclause contained in Clause AA.2. 

This document applies to the basic safety and essential performance of an EMS ventilator in combination 
with its accessories, hereafter also referred to as ME equipment: 

  • intended for patients who need differing levels of support from artificial ventilation including 
  • ventilator-dependent patients; 
  • intended to be operated by a healthcare professional operator; 
  • intended for use in the EMS environment; and 
  • intended for invasive or non-invasive ventilation. 

NOTE 2 An EMS ventilator can also be used for transport within a professional healthcare facility. 

An EMS ventilator is not considered to use a physiologic closed loop-control system unless it uses a 
physiological patient variable to adjust the artificial ventilation therapy settings. 

This document is also applicable to those accessories intended by their manufacturer to be connected to 
the ventilator breathing system, or to an EMS ventilator, where the characteristics of those accessories 
can affect the basic safety or essential performance of the EMS ventilator. 

NOTE 3 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+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1. 

NOTE 4 Additional information can be found in IEC 60601-1:2005+AMD1:2012+AMD2:2020, 4.2.  

This document does not specify the requirements for the following:  

NOTE 5 See ISO/TR 21954 for guidance on the selection of the appropriate ventilator for a given patient.  

  • ventilators or accessories intended for ventilator-dependent patients in critical care applications, which are given in ISO 80601-2-12. 
  • ventilators or accessories intended for ventilator-dependent patients in the home healthcare environment, which are given in ISO 80601-2-72.  
  • ventilators or accessories intended for anaesthetic applications, which are given in ISO 80601-2-13.  
  • ventilators or accessories intended for ventilatory support equipment (intended only to augment the ventilation of spontaneously breathing patients), which are given in ISO 80601-2-79 and ISO 80601-2-80.  
  • obstructive sleep apnoea therapy ME equipment, which are given in ISO 80601-2-70.  
  • user-powered resuscitators, which are given in ISO 10651-4.  
  • gas-powered emergency resuscitators, which are given in ISO 10651-5.  
  • continuous positive airway pressure (CPAP) ME equipment.  
  • high-frequency jet ventilators (HFJVs), which are given in ISO 80601-2-87.  

NOTE 6 An EMS ventilator can incorporate high-frequency jet or high-frequency oscillatory ventilation-modes.

  • respiratory high-flow therapy equipment, which are given in ISO 80601-2-90.

NOTE 7 An EMS ventilator can incorporate high-flow therapy operational mode, but such a mode is only for spontaneously breathing patients.

  • oxygen therapy constant flow ME equipment.
  • cuirass or “iron-lung” ventilators.

 

NOTE 7 An EMS ventilator can incorporate high-flow therapy operational mode, but such a mode is only for 
spontaneously breathing patients. 

 

 oxygen therapy constant flow ME equipment. 
 cuirass or “iron-lung” ventilators. 

 

Project need:

Project Need
To maintain alignment with international requirements (new edition of adoption, new adopted standard, new amendment of an adopted standard, etc.) The proposed New Edition/ New Amendment are being developed at the request of Technical Committees. It will provide the industry with the latest requirements for the safety testing of medical devices.

Note: The information provided above was obtained by the Standards Council of Canada (SCC) and is provided as part of a centralized, transparent notification system for new standards development. The system allows SCC-accredited Standards Development Organizations (SDOs), and members of the public, to be informed of new work in Canadian standards development, and allows SCC-accredited SDOs to identify and resolve potential duplication of standards and effort.

Individual SDOs are responsible for the content and accuracy of the information presented here. The text is presented in the language in which it was provided to SCC.