I.S. EN ISO 80601-2-69:2020
Current
The latest, up-to-date edition.
Medical electrical equipment - Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2020)
Hardcopy , PDF
English
07-12-2020
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Dates of withdrawal of national standards are available from NSAI.
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Foreword
Introduction
201. 1 * Scope, object and related standards
201. 2 Normative references
201. 3 Terms and definitions
201. 4 General requirements
201. 5 General requirements for testing of ME equipment
201. 6 Classification of ME equipment and ME systems
201. 7 ME equipment identification, marking and documents
201. 8 Protection against electrical hazards from ME equipment
201. 9 Protection against mechanical hazards of ME equipment and ME systems
201. 10 Protection against unwanted and excessive radiation hazards
201. 11 Protection against excessive temperatures and other hazards
201. 12 Accuracy of controls and instruments and protection against hazardous outputs
201. 13 Hazardous situations and fault conditions for ME equipment
201. 14 Programmable electrical medical systems (PEMS)
201. 15 Construction of ME equipment
201. 16 ME systems
201. 17 Electromagnetic compatibility of ME equipment and ME systems
201.101 Outlet connector
201.102 Requirements for parts and accessories
201.103 Functional connection
201.104 * Indication of duration of operation
201.105 Integrated conserving equipment function
202 Electromagnetic disturbances – Requirements and tests
206 Usability
211 Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
Annex C (informative) Guide to marking and labelling requirements for ME equipment and ME systems
Annex D (informative) Symbols on marking
Annex AA (informative) Particular guidance and rationale
Annex BB (informative) Reference to the IMDRF essential principles and labelling guidances
Annex CC (informative) Reference to the essential principles
Annex DD (informative) Reference to the general safety and performance requirements
Annex EE (informative) Terminology — alphabetized index of defined terms
Bibliography
This document specifies requirements for the basic safety and essential performance of an oxygen concentrator in combination with its accessories, hereafter referred to as ME equipment, intended to increase the oxygen concentration of gas intended to be delivered to a single patient.
| Committee |
TC 121
|
| DocumentType |
Standard
|
| Pages |
82
|
| ProductNote |
The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| EN ISO 80601-2-69:2020 | Identical |
| ISO 80601-2-69:2020 | Identical |
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