ISO 9919:2005

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

Publication date:   Mar 15, 2005

95.99 Withdrawal of Standard   Mar 16, 2011

General information

95.99 Withdrawal of Standard   Mar 16, 2011

ISO

ISO/TC 121/SC 3 Respiratory devices and related equipment used for patient care

International Standard

11.040.10   Anaesthetic, respiratory and reanimation equipment

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Scope

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.

Life cycle

PREVIOUSLY

WITHDRAWN
ISO 9919:1992

NOW

WITHDRAWN
ISO 9919:2005
95.99 Withdrawal of Standard
Mar 16, 2011

REVISED BY

WITHDRAWN
ISO 80601-2-61:2011