ISO 26782:2009
Anaesthetic and respiratory equipment — Spirometers intended for the measurement of time forced expired volumes in humans
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.
| Get this standard | Prices exclude GST | |
|---|---|---|
| PDF ( Single user document) |
$281.74 NZD
|
|
| HardCopy |
$319.13 NZD
|
|
| Networkable PDF |
Price varies
|
*Scope
Normative references
Terms and definitions
General requirements
Electrical safety
Mechanical safety
Identification, marking and documents
Marking of the scale or display
Legibility of markings
Durability of markings
Marking of the spirometer or its packaging
Instructions for use
General
Cleaning, disinfection and sterilization
Technical description
*Measurement range
Performance requirements
Accuracy
Recording time
Graphical display aspect ratios
Volume recording
*Start of forced exhalation
*End of forced exhalation
Linearity
Repeatability
Expiratory impedance
Constructional requirements
Effects of dropping components of a hand-held spirometer or
Calibration
Dismantling and re-assembly
Cleaning, sterilization and disinfection
Re-usable spirometer and parts
Spirometer and parts requiring processing before use
Spirometer and parts delivered sterile
Biocompatibility
Keep me up-to-date
Register to receive notifications when updates are made to this standard.
Related Information
Similar Standards
-
AS/NZS 3200.2.4:2006
Approval and test specification - Medical electrical equipment - Particular requirements for safety - Cardiac defibrillators
-
AS/NZS IEC 60601.2.20:2022 (RLV)
Medical electrical equipment, Part 2.20: Particular requirements for the basic safety and essential performance of infant transport incubators
-
AS/NZS IEC 60601.2.21:2015
Medical electrical equipment - Part 2.21: Particular requirements for the basic safety and essential performance of infant radiant warmers -
BS 341-2:1963
Transportable gas container valves, Valves with taper stems for use with breathing apparatus
*Scope
Normative references
Terms and definitions
General requirements
Electrical safety
Mechanical safety
Identification, marking and documents
Marking of the scale or display
Legibility of markings
Durability of markings
Marking of the spirometer or its packaging
Instructions for use
General
Cleaning, disinfection and sterilization
Technical description
*Measurement range
Performance requirements
Accuracy
Recording time
Graphical display aspect ratios
Volume recording
*Start of forced exhalation
*End of forced exhalation
Linearity
Repeatability
Expiratory impedance
Constructional requirements
Effects of dropping components of a hand-held spirometer or
Calibration
Dismantling and re-assembly
Cleaning, sterilization and disinfection
Re-usable spirometer and parts
Spirometer and parts requiring processing before use
Spirometer and parts delivered sterile
Biocompatibility