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This document specifies a procedure for a chamber test with different options of chamber sizes to measure the formaldehyde concentrations in air from wood products under defined test conditions of temperature, relative humidity, loading and air exchange rate. Results obtained from this small-scale chamber test method can be used for quality control (factory production control – ‘FPC’) based on correlation established by reference chamber test methods according to ISO, EN or ASTM standards. The establishment of a correlation is described in Annex D.

 

This document specifies the commonly used terms in mine drainage.

 

This part of ISO/IEC 23090 specifies an architecture and data model for interchange of scene-based media for use in systems and applications that employ renderers for the presentation of immersive media, including audio, visual, tactile and other representations of media types. Clients of such systems and applications are referred to as render-based clients. At the core of the model is a vocabulary of terms and definitions that can be used to annotate a scene graph or scene asset with metadata, i.e., to facilitate the translation of media from one format to another. Such translation from one format to another format is a commonly encountered challenge in the distribution of scene-based media, as a number of formats have emerged to gain popularity in various application areas, e.g., gaming, social media, e-commerce, and content production. The corresponding vocabulary of terms and definitions describes nodes, media formats, media attributes, and render processing instructions of commonly-used scene graph formats and media representations. This collection of terms and definitions is referred to as the Independent Mapping Space (IMS). Elements from the Independent Mapping Space may be used to annotate a scene graph or media format so that its translation to another format is more straightforward and consistently performed. Thus, the IMS facilitates the distribution and interoperability of a variety of scene-based media into render applications that are limited in the types of formats that they are designed to support. Such render applications are anticipated to serve an essential role in the emerging Metaverse.

 

This document specifies a method for the determination of the time-weighted average mass concentration of soluble particulate fluorides and hydrofluoric acid (HF) in workplace air by collection of the particulate fluorides on a pre-filter and HF on an alkali-impregnated filter and analysis by ion chromatography. This method is only applicable to determination of particulate fluorides that are soluble using the sample preparation procedure specified. For aerosol sampling, this method is applicable to the personal sampling of the inhalable fraction of airborne particles, as defined in ISO 7708, and to static (area) sampling. The method is applicable to the determination of masses of 0,005 mg to at least 1,25 mg of particulate fluorides per sample and 0,015 mg to at least 1,2 mg of HF per sample. The concentration range of particulate fluorides and HF in air for which the measuring procedure is applicable is determined by the sampling method selected by the user. For a 120 l air sample, the measuring range is approximately 0,04 mg/m3 to at least 10 mg/m3 for particulate fluorides and approximately 0,13 mg/m3 to at least 10 mg/m3 for HF. HF can react with co-sampled particulate matter on the pre-filter, causing an interference on the measured concentration.

 

This part of ISO 9276 specifies guidelines and instructions for the graphical representation of particle size analysis data in histograms, distribution densities and cumulative distributions. It also establishes a standard nomenclature to be followed to obtain the distributions mentioned above from measured particle size data. This part of ISO 9276 applies to the graphical representation of particle size distributions of solid particles, droplets or gas bubbles covering all size ranges.

 

This document specifies requirements and associated test methods for assistive products for toileting, bathing and showering (from herein referred as ‘assistive product’ within the standard) and which are considered to be medical devices, intended by the manufacturer to alleviate or compensate for disability. The standard specifies safety, functional and ergonomic requirements for both persons with disability and assistants that apply during normal use and foreseeable misuse and failure. This document specifies requirements and test methods for assistive products within the following divisions of EN ISO 9999:2022. There are no specific requirements and test methods for products marked with *. Only the relevant general requirements apply when these products are considered to be medical devices. This document does not apply for:

 

This document provides information on the implementation of the reference and conformance software associated with ISO/IEC 23090-31, "Coded representation of immersive media - Part 31: Haptics coding". The document specifies a set of tests and procedures designed to indicate whether encoders or decoders meet the requirements specified in ISO/IEC 23090-31.

 

 

This document is applicable to the evaluation of a substrate's resistance to absorption of a selected series of liquid hydrocarbons of different surface tensions. This document is intended to provide a guide to oil stain resistance. It can provide a rough index of oil stain resistance as, generally, the higher the oil repellency grade, the better resistance to staining by oily materials, especially liquid oil substances. This is particularly true when comparing various finishes for a given substrate. This International Standard can also be utilized in determining if washing and/or drycleaning treatments have any adverse effect on the oil repellency characteristics of a substrate. This document is not intended to give an absolute measure of the resistance of the substrate to staining by all oily materials. Other factors, such as composition and viscosity of the oily substances, substrate construction, fibre type, dyes and other finishing agents, also influence stain resistance. This International Standard is not intended to estimate the resistance to penetration of the substrate by oil-based chemicals.

 

This document provides general requirements of Manufacturing Readiness Review (MRR) for deliverable space products (sometimes named Production Readiness Review), including initiate process of MRR, implement process of MRR and activities after MRR. This document is applicable to Manufacturing Readiness Review of deliverable space products. The MRR could be repeated during the manufacturing phase for each repetitive item and first manufactured item.

 

This document specifies the abstract class of a media thing (MThing), a basic component to construct the Internet of media things. The MThing class contains the basic APIs to:

 

This document specifies requirements and includes guidance for the verification of declared sustainability information, including information presented in quantitative and qualitative formats.

 

This document provides reference software for ISO/IEC 23090-05 as an electronic attachment.

 

 

This document specifies requirements for the contents of a technical file to demonstrate the fulfilment of regulatory requirements for an endosseous dental implant that may include: This document includes requirements for intended use and performance, design attributes, components, biocompatibility, manufacturing, packaging, sterilization, shelf life, marking, labelling and information supplied by the manufacturer. The following devices are not included within the scope of this document:

 

 

This document specifies a method [1] for the quantitative determination of saxitoxin (STX), decarbamoyl saxitoxin (dcSTX), neosaxitoxin (NEO), decarbamoyl neosaxitoxin (dcNEO), gonyautoxin 1 and 4 (GTX1,4; sum of isomers), gonyautoxin 2 and 3 (GTX2,3; sum of isomers), gonyautoxin 5 (GTX5 also called B1), gonyautoxin 6 (GTX6 also called B2), decarbamoyl gonyautoxin 2 and 3 (dcGTX2,3; sum of isomers), N sulfocarbamoyl gonyautoxin 2 and 3 (C1,2; sum of isomers) and N-sulfocarbamoyl gonyautoxin 1 and 4 (C3,4; sum of isomers) in (raw) mussels, oysters, scallops and clams. Laboratory experience has shown that this document can also be applied to other marine invertebrates [2], [3] and processed products of those species, however, no complete interlaboratory validation study according to ISO 5725 2:1994 has been carried out so far. The method described was validated in an interlaboratory study [4], [5] and was also verified in a European Union Reference Laboratory for Marine Biotoxins (EURLMB)-performance test aiming the total toxicity of the samples [6]. Toxins which were not available in the first interlaboratory study [4], [5] as dcGTX2,3 and dcNEO were validated in two additional interlaboratory studies [7], [8]. The lowest validated levels [4], [5], [8], are given in µg toxin (free base)/kg shellfish tissue and also as µmol/kg shellfish tissue and are listed in Table 1. [Table 1] A quantitative determination of GTX6 was not included in the first interlaboratory study but several laboratories detected this toxin directly after solid phase extraction with ion-exchange (SPE-COOH) clean-up and reported a mass concentration of 30 µg/kg or higher in certain samples. For that reason, the present method is applicable to quantify GTX6 directly, depending on the availability of the standard substance. Whenever GTX6 standard is not commercially available, it is possible to determine GTX6 after hydrolysis of Fraction 2 of the SPE-COOH clean-up, described in 6.4, as NEO. The indirect quantification of GTX6 was validated in two additional interlaboratory studies [7], [8]. A study to compare direct and indirect GTX6 quantification was conducted at the EURLMB [16]. A quantitative determination of C3,4 was included in the first interlaboratory study. The present method is applicable to quantify C3,4 directly, depending on the availability of the standard substance. If no standard substances are available, C3,4 can only be quantified as GTX1,4 if the same hydrolysis protocol used for GTX6 (6.4) is applied to Fraction 1 of the SPE-COOH clean-up [10]. A study to compare direct and indirect C3,4 quantification was conducted at the EURLMB [16].

 

This document specifies general principles and requirements for the validation and verification process of sustainability information, including reporting on environmental, social, governance (ESG) and other sustainability aspects. It provides general principles and requirements for determining the categorization of quantitative and qualitative information. These principles and requirements contribute to the set of rules and procedures that are provided in validation/verification programmes. This document can also be used as the basis for validation and verification activities that support other conformity assessment schemes. NOTE: This document can be applied by validation and verification bodies according to ISO/IEC 17029. It can contribute to schemes operated by inspection bodies according to ISO/IEC 17020 or certification bodies according to ISO/IEC 17065.

 

 

This document specifies requirements and associated test methods for assistive products for toileting, bathing and showering (from herein referred as ‘assistive product’ within the document) and which are considered to be medical devices, intended by the manufacturer to alleviate or compensate for disability. NOTE Assistive products are considered to be medical devices in some jurisdictions but not in others. The work environment and safety aspects for assistants are also included. It specifies safety and performance requirements that apply during normal use and foreseeable misuse and failure. It also specifies methods of measurement of the forces necessary to operate controls and specifies limits on the forces needed for some operations. This document specifies requirements and test methods for assistive products within the following divisions of ISO 9999: 09 12 03 Commode chairs; 09 12 06 Toilets; 09 12 09 Toilet seats; 09 12 10 Toilet splash guards; 09 12 12 Raised toilet seats mounted on frame; 09 12 15 Toilet seats inserts; 09 12 18 Raised toilet seats fixed to toilet; 09 12 21 Toilet seats with built-in raising mechanism to help standing up and sitting down; 09 12 24 Toilet arm supports and toilet back supports mounted on toilet; 09 12 25 Toilet arm supports and toilet back supports, free standing; 09 12 36 Douches and air dryers for attachment to a toilet; 09 33 04 Bath boards 09 33 05 Bath seats 09 33 07 Shower chairs with and without wheels 09 33 08 Back supports for bath or shower 09 33 12 Bathing stretchers, shower tables and diaper-changing tables; NOTE: Mainstream diaper-changing tables for babies/toddlers are excluded. They are covered by EN 12221-1 and EN 12221-2. 09 33 15 Wash basins NOTE: General requirements for wash basins are covered by EN 14688. 09 33 18 Bidets 09 33 21 Bathtubs 09 33 36 Assistive products for drying oneself 18 15 06 Height adjustable plinths and brackets; 18 18 03 Handrails and support rails; 18 18 06 Fixed grab bars and handgrips; 18 18 10 Removable grab rails and handgrips; 18 18 11 Hinged rails and arm supports; This document does not encompass requirements regarding: — safe mounting in building structures; — fixed building installations e.g. water, electricity, drainage and sewerage, requirements in relation to excretion-disposal and -wrapping systems; — 12 36 15 bathtub hoists that are covered by ISO 10535; — 09 33 21 Bathtubs — stability and friction issues in relation to slippery surfaces due to soap; — products that have been customised or custom-made for an individual user. NOTE: this list is based on ISO 9999:2016, however in the revision process, this will be updated to corresponding codes of ISO 9999:2022