ISO 9919:2005

Medical electrical equipment — Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use

Medical electrical equipment — Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use

Digital Document2005 edition2005Purchase Options

Referenced standards

IEC 60068-2-27:1987IEC 60068-2-32:1975IEC 60068-2-64:1993IEC 60068-2-6:1995IEC 60079-4:1975IEC 60529:2001IEC 60601-1-1:2000IEC 60601-1-2:2001IEC 60601-1-4:1996IEC 60601-1-6:2004IEC 60601-1-8:2003IEC 60601-1:1988IEC 60825-1:2001IEC 60825-2:2000ISO 14155-1:2003ISO 14155-2:2003ISO 14937:2000ISO 15223:2000
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ISO 9919:2005

Medical electrical equipment — Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use

Medical electrical equipment — Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use

For the purposes of ISO 9919:2005, the Scope given in IEC 60601-1:1988 (Clause 1) applies, except as follows.

Amendment (add at the end of 1.1):

ISO 9919:2005 specifies particular requirements for the basic safety and essential performance of pulse oximeter equipment intended for use on humans. This includes any part necessary for normal use, e.g. the pulse oximeter monitor, pulse oximeter probe, probe cable extender.

These requirements also apply to pulse oximeter equipment, including pulse oximeter monitors, pulse oximeter probes and probe cable extenders, that has been reprocessed.

The intended use of pulse oximeter equipment includes, but is not limited to, the estimation of arterial oxygen haemoglobin saturation and pulse rate on patients in healthcare institutions as well as on patients in home care.

ISO 9919:2005 is not applicable to pulse oximeter equipment intended for use in laboratory research applications nor to oximeters that requires a blood sample from the patient.

ISO 9919:2005 is not applicable to pulse oximeter equipment solely intended for fetal use.

ISO 9919:2005 is not applicable to remote or slave (secondary) devices that display SpO2 values that are located outside of the patient environment.

The requirements of ISO 9919:2005 which replace or modify requirements of IEC 60601-1:1988 and its Amendments 1 (1991) and 2 (1995) are intended to take precedence over the corresponding general requirements.

Edition2005
Published Date2005
Published ByInternational Standardization Organisation
Page Count81