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UNE-EN ISO 23747:2016

Current
Current

The latest, up-to-date edition.

Anaesthetic and respiratory equipment - Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans (ISO 23747:2015)
Available format(s)

Hardcopy , PDF

Language(s)

Spanish, Castilian, English

Published date

20-01-2016

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
    4.1 Safety for PEFMs that utilize electricity
    4.2 Mechanical safety for all PEFMs
5 Identification, marking and documents
    5.1 Marking of the scale or display
    5.2 Marking of PEFM or packaging
    5.3 Instructions for use
    5.4 Technical description
6 PEFM measurement range
7 Performance requirements
    7.1 Error of measurement
    7.2 Linearity
    7.3 Resistance to flow
    7.4 Frequency response
8 Dismantling and reassembly
9 Effects of mechanical ageing
10 Effects of dropping a hand-held PEFM
11 Cleaning, sterilization and disinfection
    11.1 Re-usable PEFM and parts
    11.2 PEFM and parts delivered sterile
12 Compatibility with substances
13 Biocompatibility
Annex A (informative) Rationale for tests and examples of
                       test apparatus
Annex B (normative) Determination of error, repeatability and
                       resistance to PEFM output
Annex C (normative) Determination of frequency response
Annex D (normative) Test methods for determination of the effects
                       of dismantling, ageing and dropping
Annex E (informative) Environmental aspects
Annex F (informative) Reference to the essential principals
Annex ZA (informative) Relationship between this International
                       Standard and the Essential Requirements
                       of EU Directive 93/42/EEC
Bibliography

Defines requirements for peak expiratory flow meters (PEFMs) intended for the assessment of pulmonary function in spontaneously breathing humans.

Committee
CTN 110
DevelopmentNote
Supersedes UNE EN 13826. (01/2008)
DocumentType
Standard
Pages
40
PublisherName
Asociacion Espanola de Normalizacion
Status
Current
Supersedes

ISO 128-40:2001 Technical drawings General principles of presentation Part 40: Basic conventions for cuts and sections
ISO/IEC TR 10000-1:1998 Information technology Framework and taxonomy of International Standardized Profiles Part 1: General principles and documentation framework
ISO 10241:1992 International terminology standards Preparation and layout
ISO 690:2010 Information and documentation Guidelines for bibliographic references and citations to information resources
ISO 128-34:2001 Technical drawings General principles of presentation Part 34: Views on mechanical engineering drawings
IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
ISO 14937:2009 Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
ISO 690-2:1997 Information and documentation Bibliographic references Part 2: Electronic documents or parts thereof
ISO/TR 16142:2006 Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
ISO 128-44:2001 Technical drawings General principles of presentation Part 44: Sections on mechanical engineering drawings
ISO 128-30:2001 Technical drawings General principles of presentation Part 30: Basic conventions for views
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 14971:2007 Medical devices Application of risk management to medical devices
ISO 15223-1:2016 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements

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