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

 

 

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 a guideline to the implementation of the specific space profiles for VSEs specified in the ISO/IEC 29110-6-1 through a set of development processes. Industry and large organisations recognize the value of VSEs, i.e., enterprises, organisations (e.g., government agency, non-profit organisation), projects or departments with up to 25 people, in contributing with emerging new technology that bigger organisations cannot use them as easily nor incorporate them in their solutions as fast. But often these VSEs are not ready to comply with the stringent requirements for space projects. The purpose of this document is to ultimately achieve the process capacity to participate in the development of critical software in the space domain. But not all software in the space domain can be addressed. For example, for software embedded in products that can be fatal to human life, additional safeguards will be required. VSE in space domain can demonstrate the quality in their processes in a stepwise approach to eventually participate in space projects in a faster and feasible way This document is targeted at small suppliers, developers, managers, and quality assurance managers of software products in the space domain. The document may also be used by a single party through a self-imposed set of processes. This document does not prescribe a specific system or software life cycle model, development methodology, model or technique. The users of this document select the processes to be deployed and map them onto the specific project life cycle model. The parties are also responsible for selecting and applying the software development methods and for performing the activities and tasks suitable for the software project. This document is not intended to conflict with any organization's policies, procedures, and standards or with any national laws and regulations. Any such conflict should be resolved before using this document. The processes in this document are contained in Clauses 6, 7, 8 and 9 presented in their correspondent groups as per the ISO/IEC 29110-6-1 respectively. It is recognised that specific projects or organizations may not need to use all the processes provided by this document. Therefore, implementation of this document typically involves selecting a set of processes suitable to the organization or project and will so be reflected in the project plan of each project.

 

 

 

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

 

This document specifies the conditions for the visual inspection of domestic articles made from ceramic, glass, glass ceramic, decorated glass, vitreous enamel, coatings, rubber, silicones, metal, and plastics after testing its dishwashing resistance according to the procedures described in the relevant parts of the EN 12875 series.

 

This European Standard specifies a method for testing the resistance of domestic articles made from ceramic, glass, glass ceramic, vitreous enamel, metal and plastics under the combined chemical, thermal and mechanical stresses of mechanical dishwashing in domestic dishwashers. It specifies a reference test method for domestic dishwashing only. It does not define the number of dishwashing cycles which any given product shall withstand.

 

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 the dimensions, tolerances and the required characteristics of a quick release, self retaining, positive locking, double acting pin with button handle for aerospace application.

 

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].