ISO 26782:2009
Current
The latest, up-to-date edition.
Anaesthetic and respiratory equipment — Spirometers intended for the measurement of time forced expired volumes in humans
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07-09-2009
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ISO 26782:2009 specifies requirements for spirometers intended for the assessment of pulmonary function in humans weighing more than 10 kg.
ISO 26782:2009 applies to spirometers that measure timed forced expired volumes, either as part of an integrated lung function device or as a stand-alone device, irrespective of the measuring method employed.
| Committee |
ISO/TC 121/SC 3
|
| DevelopmentNote |
Supersedes ISO/DIS 26782. (07/2009)
|
| DocumentType |
Standard
|
| Pages |
27
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Standards | Relationship |
| IS/ISO 26782 : 2009 | Identical |
| SN EN ISO 26782:2010 | Identical |
| GOST R ISO 26782 : 2016 | Identical |
| NF EN ISO 26782 : 2009 | Identical |
| AAMI ISO 26782 : 2015 | Identical |
| NBN EN ISO 26782 : 2009 COR 2009 | Identical |
| NEN EN ISO 26782 : 2009 C1 2009 | Identical |
| NS EN ISO 26782 : 2009 AC 2009 | Identical |
| I.S. EN ISO 26782:2009 | Identical |
| PN EN ISO 26782 : 2009 AC 2010 | Identical |
| SN EN ISO 26782 : 2010 CORR 2010 | Identical |
| UNI EN ISO 26782 : 2009 | Identical |
| UNE-EN ISO 26782:2010 | Identical |
| BS EN ISO 26782:2009 | Identical |
| DIN EN ISO 26782:2010-02 | Identical |
| 16/30295446 DC : 0 | BS ISO 19223 - LUNG VENTILATORS AND RELATED EQUIPMENT - VOCABULARY AND SEMANTICS |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| ISO 23747:2015 | Anaesthetic and respiratory equipment Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans |
| 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/TR 16142:2006 | Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices |
| PD 6461-1:1995 | General metrology Basic and general terms (VIM) |
| 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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