Medical electrical equipment — Clinical performance evaluation of clinical thermometers
This document specifies the requirements and methods for the clinical investigation of ME equipment used to measure the body temperature in indirect measurement mode.
This document covers both intermittently and continuously measuring clinical thermometers.
NOTE For clinical thermometers in direct measurement mode determining the technical accuracy in accordance with IEC 80601-2-56 is…
Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential per...
ISO 80601-2-61:2017 applies to the basic safety and essential performance of pulse oximeter equipment intended for use on humans, hereafter referred to as me equipment. This includes any part necessary for normal use, including the pulse oximeter monitor, pulse oximeter probe, and probe cable extender.
These requirements also apply to pulse oximeter equipment, including pulse oximeter monitors,…
Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for urine ...
This document specifies requirements and provides recommendations for the pre-examination phase of cell free DNA (cfDNA) from body fluid specimens other than blood, including but not limited to the collection, handling, storage, transport, processing and documentation of human body fluids, such as urine, cerebrospinal fluid (CSF), pleural effusions and saliva, intended for cfDNA examination.…
Water quality — Determination of the dioxin-like activity of water and wastewater — Method using in ...
This document specifies a method for the determination of the dioxin‑like activity of water and wastewater by means of an AhR‑mediated reporter gene assay utilizing stably transfected mammalian cell line. This reporter gene assay is based on the activation of the mammalian AhR signalling pathway.
This method is applicable to:
— drinking water;
— fresh water;
— groundwater…
Plastics — Determination of the aerobic biodegradation of plastic materials exposed to seawater usin...
This document describes a laboratory test method to determine the aerobic biodegradation of plastic materials exposed to seawater using accelerated conditions.
Furthermore, this document describes the general requirements of the apparatus and the procedures for using this test method. The biodegradation is determined by measuring the oxygen demand in a closed respirometer or by measuring the CO2…
Fans — Determination of fan sound power levels under standardized laboratory conditions — Part 3: En...
ISO 13347-3:2004 applies to industrial fans as defined in ISO 5801 and ISO 13349. It is limited to the determination of airborne sound emission for the specified set-ups. Vibration is not measured, nor is the sensitivity of airborne sound emission to vibration effects determined.
The sizes of fan which can be tested in accordance with ISO 13347-3:2004 are limited only by the practical aspects of…
Fans — Determination of fan sound power levels under standardized laboratory conditions — Part 2: Re...
ISO 13347-2:2004 gives a detailed description of reverberant room methods for the determination of fan sound power levels. It is for use under standardized laboratory conditions and recognises that tests in situ are subject to increased uncertainty. These test procedures are not necessarily appropriate to site test conditions. Acoustic system effects are presently the subject of considerable…
Protective clothing — Protection against chemicals — Determination of resistance of protective cloth...
ISO 6529:2013 describes laboratory test methods to determine the resistance of materials used in protective clothing, including gloves and including footwear, when the footwear is an integral part of the clothing, to permeation by liquid or gaseous chemicals under the conditions of either continuous or intermittent contact.
Method A is applicable to testing against liquid chemicals, either…
