Plastiques alvéolaires rigides — Détermination des caractéristiques de compression
Le présent document spécifie des méthodes permettant de déterminer la résistance à la compression et la déformation relative correspondante, la contrainte en compression correspondant à 10 % de déformation relative et le module en compression des plastiques alvéolaires rigides.
Medical electrical equipment — Part 2-30: Particular requirements for basic safety and essential per...
IEC 80601-2-30:2018 applies to the basic safety and essential performance of automated sphygmomanometers, hereafter referred to as ME equipment, which by means of an inflatable cuff, are used for non continuous indirect estimation of the blood pressure without arterial puncture. This document specifies requirements for the basic safety and essential performance for this ME equipment and its…
Appareils électromédicaux — Partie 2-30: Exigences particulières de sécurité de base et de performan...
L’IEC 80601-2-30:2018 s'applique à la sécurité de base et aux performances essentielles des sphygmomanomètres automatiques, ci-après dénommés appareils EM, qui, au moyen d'un brassard gonflable, sont utilisés pour l'estimation indirecte non continue de la pression artérielle sans ponction artérielle. Le présent document spécifie les exigences pour la sécurité de base et…
Rubber, vulcanized — Quantitative analysis methods for volatilized sulfur and sulfur compounds under...
This document specifies methods for determining the amount of sulfur compounds volatilized from vulcanized rubber under heating conditions using gas chromatograph (GC) or ion chromatograph (IC). The methods apply to the sulfur compounds which are hydrogen sulfide (H2S), carbonyl sulfide (COS), carbon disulfide (CS2) and sulfur dioxide (SO2).
The methods cannot be used above the thermal…
Assistive products for tissue integrity when lying down — Part 4: Test methods for durability
This part of ISO 20342 specifies conditions and test methods for the durability of assistive products for tissue integrity (APTI) when lying down additional to ISO 20342-1.
This document is applicable to APTIs, such as mattresses and overlays, and includes single patient multiple use products.
This document does not apply to single use products.
NOTE It is intended to…
Ophthalmic optics — Contact lenses and contact lens care products — Determination of preservative up...
ISO 11986:2017 provides general procedures for the selection of methods, preparation of samples, and the conduct of testing for the uptake and release of preservatives from contact lenses.
NOTE 1 Due to the manifest difficulties of reproducibility when coating contact lenses with mineral and organic deposits encountered during lens wear, these methods are only applicable to new and unused…
Traditional Chinese medicine — Isatis indigotica root
This document specifies the minimum requirements and test methods for Isatis indigotica root derived from the plant Isatis indigotica Fort.
It is applicable to Isatis indigotica roots that are sold as Chinese material medica (whole medicinal materials) and decoction pieces derived from this plant.
Atomic layer deposition — Chemical characteristics and related process specifications of atomic laye...
This document describes the chemical characteristics and related process specifications of the atomic layer deposition precursors, including assay content, metal purity, and anion content specification.
Fine bubble technology — Characterization of ultrafine bubbles — Part 1: Data correction to exclude ...
This document specifies the evaluation method for size and concentration indices of ultrafine bubbles including the data correction to exclude particulate contaminants using the blank water.It is only applicable to ultrafine bubble dispersion (UFBD) in water.
Air filters for general ventilation — Part 1: Technical specifications, requirements and classificat...
ISO 16890-1:2016 establishes an efficiency classification system of air filters for general ventilation based upon particulate matter (PM). It also provides an overview of the test procedures, and specifies general requirements for assessing and marking the filters, as well as for documenting the test results. It is intended for use in conjunction with ISO 16890‑2, ISO 16890‑3 and ISO 16890‑4.…
