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)

German, English

Published date

01-01-2015

Publisher

German Institute for Standardisation (Deutsches Institut für Normung)

DevelopmentNote	Supersedes DIN EN 13826. (10/2007)
DocumentType	Standard
Pages	38
PublisherName	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Current

Standards	Relationship
SN EN ISO 23747:2015	Identical
NEN EN ISO 23747 : 2015	Identical
NF EN ISO 23747 : 2015	Identical
ISO 23747:2015	Identical
NBN EN ISO 23747 : 2015	Identical
I.S. EN ISO 23747:2015	Identical
BS EN ISO 23747:2015	Identical
UNE-EN ISO 23747:2016	Identical
NS EN ISO 23747 : 2015	Identical
EN ISO 23747:2015	Identical

DIN EN ISO 26782:2010-02

Anaesthetic and respiratory equipment - Spirometers intended for the measurement of time forced expired volumes in humans (ISO 26782:2009 + Cor. 1:2009) (includes Corrigendum AC:2009)

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
DIN EN ISO 15223-1:2015-08 (Draft)	MEDICAL DEVICES - SYMBOLS TO BE USED WITH MEDICAL DEVICE LABELS, LABELLING AND INFORMATION TO BE SUPPLIED - PART 1: GENERAL REQUIREMENTS (ISO 15223-1:2016, CORRECTED VERSION 2017-03)
DIN EN ISO 13485:2016-08	Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
ISO 128-34:2001	Technical drawings General principles of presentation Part 34: Views on mechanical engineering drawings
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
DIN EN ISO 14971:2013-04	MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007)
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
DIN ISO 690:2013-10	INFORMATION AND DOCUMENTATION - GUIDELINES FOR BIBLIOGRAPHIC REFERENCES AND CITATIONS TO INFORMATION RESOURCES (ISO 690:2010)