Toimialayhteisöt

 

This document specifies the classification for commercial beverage coolers and their requirements and test methods. This document is applicable to integral refrigeration systems. This document is not applicable to remote and secondary system cabinets.

 

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 typically sufficient. This document specifies additional disclosure requirements. This document is not applicable to the clinical investigation of a screening thermographs for human febrile temperature screening whose laboratory accuracy requirements are described in IEC 80601-2-59.

 

This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in 201.3.220, hereafter also referred to as ME equipment or ME system, in combination with its accessories: —   intended for use with patients who can breathe spontaneously; and —   intended for patients who would benefit from improved alveolar gas exchange; and who would benefit from receiving high-flow humidified respiratory gases, which can include a patient whose upper airway is bypassed. EXAMPLE 1 Patients with Type 1 Respiratory Failure who exhibit a reduction in arterial blood oxygenation. EXAMPLE 2 Patients who would benefit from reduced work of breathing, as needed in Type 2 Respiratory Failure, where arterial carbon dioxide is high. EXAMPLE 3 Patients requiring humidification to improve mucociliary clearance. Respiratory high-flow therapy equipment can be intended for use in the home healthcare environment or intended for use in professional healthcare facilities. NOTE 1        In the home healthcare environment, the supply mains is often not reliable. Respiratory high-flow therapy equipment can be: —   fully integrated ME equipment; or —   a combination of separate items forming a ME system. This standard also applies to other types of respiratory equipment when that equipment includes a respiratory high-flow therapy mode. NOTE 2  This standard and ISO 80601-2-12[14] are applicable to a critical care ventilator with a high-flow therapy mode. Respiratory high-flow therapy equipment can be transit-operable. This document is also applicable to those accessories intended by their manufacturer to be connected to the respiratory high-flow therapy equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the respiratory high-flow therapy equipment. EXAMPLE 4         Breathing sets, connectors, humidifier, breathing system filter, external electrical power source, distributed alarm system, high-flow nasal cannula, tracheal tube, tracheostomy tube, face mask and supra-laryngeal airway. If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant. Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in the general standard, 7.2.13 and 8.4.1. NOTE 3        Additional information can be found in the general standard, 4.2. This document does not specify the requirements for: —    ventilators or accessories for ventilator-dependent patients intended for critical care applications, which are given in ISO 80601-2-12[14]; —    ventilators or accessories intended for anaesthetic applications, which are given in ISO 80601-2-13[15]; —    ventilators or accessories intended for the emergency medical services environment, which are given in ISO 80601-2-84[20]; —    ventilators or accessories intended for ventilator-dependent patients in the home healthcare environment, which are given in ISO 80601-2-72[17]; —    ventilatory support equipment or accessories intended for patients with ventilatory impairment, which are given in ISO 80601-2-79[18]; —    ventilatory support equipment or accessories intended for patients with ven

 

This document applies to the basic safety and essential performance of a humidifier, also hereafter referred to as ME equipment, in combination with its accessories, the combination also hereafter referred to as ME system. This document is also applicable to those accessories intended by their manufacturer to be connected to a humidifier where the characteristics of those accessories can affect the basic safety or essential performance of the humidifier. EXAMPLE 1         Heated breathing tubes (heated-wire breathing tubes) or ME equipment intended to control these heated breathing tubes (heated breathing tube controllers). NOTE 1        Heated breathing tubes and their controllers are ME equipment and are subject to the requirements of IEC 60601-1. NOTE 2        ISO 5367 specifies other safety and performance requirements for breathing tubes. This document includes requirements for the different medical uses of humidification, such as invasive ventilation, non-invasive ventilation, nasal high-flow therapy, and obstructive sleep apnoea therapy, as well as humidification therapy for tracheostomy patients. NOTE 3        A humidifier can be integrated into other equipment. When this is the case, the requirements of the other equipment also apply to the humidifier. EXAMPLE 2         Heated humidifier incorporated into a critical care ventilator where ISO 80601-2-12[10] also applies. EXAMPLE 3         Heated humidifier incorporated into a homecare ventilator for dependent patients where ISO 80601-2-72[12] also applies. EXAMPLE 4         Heated humidifier incorporated into sleep apnoea therapy equipment where ISO 80601-2-70[11] also applies. EXAMPLE 5         Heated humidifier incorporated into ventilatory support equipment where either ISO 80601-2-79[13] or ISO 80601-2-80[14] also apply. EXAMPLE 6         Heated humidifier incorporated into respiratory high-flow therapy equipment where ISO 80601-2-90[15] also applies. This document also includes requirements for an active HME (heat and moisture exchanger), ME equipment which actively adds heat and moisture to increase the humidity level of the gas delivered from the HME to the patient. This document is not applicable to a passive HME, which returns a portion of the expired moisture and heat of the patient to the respiratory tract during inspiration without adding heat or moisture. NOTE 4        ISO 9360-1 and ISO 9360-2[4] specify safety and performance requirements for a passive HME. NOTE 5        If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant. Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1. NOTE 6        Additional information can be found in IEC 60601-1:2005+AMD1:2012+AMD2:2020, 4.2. This document does not specify the requirements for cold pass-over or cold bubble-through humidification devices, the requirements for which are given in ISO 20789[6]. This document is not applicable to equipment commonly referred to as “room humidifiers” or humidifiers used in heating, ventilation and air conditioning systems, or humidifiers incorporated into infant incubators. This

 

This document includes the sector specific requirements for the provision of private security services in the energy sector that are additional to the requirements of EN 17483 1. It specifies service requirements for quality in organization, processes, personnel and management of a security service provider and/or its independent branches and establishments under commercial law and trade as a provider with regard to security services in the energy sector. It lays down quality criteria for the delivery of security services in the energy sector requested by public and private clients. This document is suitable for the selection, attribution, awarding and reviewing of the most suitable provider of security services in the energy sector. NOTE 1 This document is the Part 4 of a series of standards on the provision of private security services for critical infrastructure. See Figure 2. [Figure 2] NOTE 2 It is important that the selection of a private security service provider always represents the best balance between quality and price. This document sets out the minimum requirements that providers are expected to comply with in order for this balance to be struck. It specifies service requirements for quality in organization, processes, personnel and management of a security service provider and/or its independent branches and establishments under commercial law and trade as a provider with regard to security services in the energy sector. It lays down quality criteria for the delivery of security services in the energy sector requested by public and private clients. This document is suitable for the selection, attribution, awarding and reviewing of the most suitable provider of security services in the energy sector. This document is not applicable to private security services in nuclear power plants. List of possible activities Activities for PSCs in CIP in the energy sector: 1. Perimeter Protection and Surveillance: — Human – reception services, static guarding, patrols, possibly K9; — Technology – CCTV, Drones, others; — Operation of a control/monitoring room; — Operation of an alarm monitoring centre; — Access Control and Management (tourniquets, barriers, authorization and badges). 2. Human and technology, e.g. use of screening and detection equipment for: — Vehicles; — Goods; — Visitors; — Staff; — Contractors (means: human and technology, e.g. use of screening and detection equipment); 3. Site and off-site Protection and Surveillance / static securing & patrolling on-site and within the building; 4. Emergency response / crisis management; — Alarm intervention; — First responders (EHS – Emergency Health Services);

 

 

 

Tämä asiakirja tarjoaa ohjeita brändisuojelutoimenpiteiden luomiseen ja täytäntöönpanoon. Se tukee brändisuojelustrategian kehittämistä ja kuvaa brändisuojelun viitekehystä tuotteiden ja asiakirjojen kehittämiseen, valmistukseen ja jakeluun. Näiden ohjeiden soveltaminen tuotteen elinkaaren aikana voi helpottaa vuorovaikutusta niiden henkilöiden ja organisaatioiden välillä, jotka osallistuvat brändisuojelutoimiin, ja tekevät suojelumenettelyistä tehokkaampia ja tarkoituksenmukaisempia. Asiakirjan tarkoituksena on tukea brändinomistajan liiketoiminnan resilienssiä, brändin mainetta ja arvoa suojaamalla tuotteita, asiakirjoja ja niihin liittyviä palveluita väärennöksiltä ja muilta loukkauksilta.

 

 

Tämä asiakirja tarjoaa ohjeita yrityksen suojaavan turvallisuuden arkkitehtuurista sekä viitekehyksestä, joka sisältää turvallisuuspolitiikat, prosessit ja kontrollityypit. Näitä tarvitaan turvallisuusriskien lieventämiseen ja hallintaan suojaavan turvallisuuden eri osa-alueilla, kuten:

 

a) turvallisuuden hallintamalli;

b) henkilöstöturvallisuus;

c) tietoturvallisuus;

d) kyberturvallisuus;

e) fyysinen turvallisuus.

 

 

Tämä asiakirja tarjoaa ohjeita organisaation resilienssipolitiikan ja -strategian suunnitteluun ja kehittämiseen. Se sisältää:

 

— ohjeita resilienssipolitiikan suunnitteluun ja laatimiseen;

— ohjeita strategian suunnitteluun resilienssipolitiikan tavoitteiden saavuttamiseksi;

— menetelmiä organisaation resilienssialoitteiden toteuttamisen priorisointiin;

— ohjeita yhteistyö- ja koordinointikyvykkyyden luomiseen resilienssin parantamiseksi.

 

Asiakirja soveltuu organisaatioille, jotka haluavat parantaa resilienssiään. Se ei ole sidottu mihinkään tiettyyn toimialaan tai sektoriin ja sitä voidaan soveltaa organisaation elinkaaren kaikissa vaiheissa resilienssin vahvistamiseksi. Tämä asiakirja ei sisällä ohjeita organisaation resilienssikyvykkyyden kehittämiseen.

 

 

 

This document specifies a method for determining by extrapolation the long-term ultimate ring bending strain and the calculation of the long-term ultimate relative ring deflection of glass-reinforced thermosetting plastics (GRP) pipes, under wet conditions. Two methods of loading are given, one using plates the other beam bars.

 

This document specifies the classification for horizontal closed ice-cream freezer with access of the product from the top via transparent or solid lid(s) and specifies their requirements and test methods. The ice-cream freezers defined in this document work with static air cooling, with a skin evaporator (no evaporator fan and no fan in the refrigerated space) and are used specifically for the storage and display of pre-packed ice-cream. This document is only applicable to integral type refrigeration systems. It is not applicable to remote and secondary system type cabinets. Ice-cream freezers defined in this document are intended to have a net volume =600 l. For transparent lid ice-cream freezers only, they are intended to have a net volume/TDA = 0,35 m.

 

 

 

This document specifies the characteristics of laminate floor coverings, supplied in modular format e.g. tiles, planks. It also specifies requirements for marking and packaging. Additional operational properties are given in Annex A.

 

This document specifies the minimum values for expected strength as a function of time and temperature in the form of reference lines, for use in calculations on polyphenylsulfone (PPSU) injection moulded fittings.

 

This document specifies a method for the measurement of effective focal spot dimensions above 0,2 µm of X-ray systems by means of the edge method applied to digital images taken from hole type or disk type gauges if no phase contrast is observed. The imaging quality and the resolution of X-ray images depend highly on the characteristics of the effective focal spot, in particular the size and the two-dimensional intensity distribution as seen from the detector plane. This document provides instructions for determining the effective size (dimensions) of standard, mini and micro focal spots of industrial X-ray tubes for users in applications where the pin hole method of ISO 32543-1 is not practicable. This determination is based on the measurement of a profile of an image of a hole or disk type gauge. The method as described in this document can be used for long term monitoring of focal spot sizes without a pin hole camera. The accuracy of this method is lower than the one of ISO 32543-1, ISO/DIS 32543-3 and the future standards in preparation, for measurements of the effective focal spot size, using ASTM hole plate IQIs (as described in ASTM E 1025, E 1742), due to its manufacturer tolerance of ±10 % of the hole diameter. It can be used by manufacturers if special hole gauges, manufactured with lower tolerance, as described in 5.2.1 are applied (see Figure 1).

 

This document gives information and guidance on the evaluation and assessment of hand-transmitted shock. For the purposes of this document, hand-transmitted shock is any impactive or impulsive vibration that the machine or tool produces as a sequence of single events (isolated shocks) linked by periods of no, or lower vibration. This document defines parameters for the evaluation of machinery emissions of hand-transmitted shocks in the frequency range covered by ISO 5349-1 (nominally 6,3 Hz to 1 250 Hz).

 

This document specifies methods for determining dimensional stability and curling (vertical deformation) of resilient floor coverings in all forms (e.g. of sheets, tiles, panels, planks or in rolls) after exposure to heat and/or after reconditioning.

 

This part of ISO 12006 defines a framework for the development of built environment classification systems. The framework is a breakdown structure supporting the spatial, physical, process aspects along with relevant resources and support This framework provides a set of recommended classification table titles for a range of information object groupings according to particular views, e.g., by form or function, supported by definitions. It shows how the object groupings classified in each table are related, e.g., in a building information model. This part of ISO 12006 applies to the complete life cycle of assets, including briefing, design, documentation, construction, operation and maintenance, demolition and possible reuse of assets or components. It applies to both building and civil engineering works, including associated engineering services, landscaping and its natural environment. It is intended for use by organizations which develop and publish such classification systems and tables, which can vary in detail to suit local needs. When this part of ISO 12006 is applied in the development of local classification systems and tables, then harmonization between them will be facilitated. The management of the built environment above the level of complex, entities and project/programmes (for example geographic catchment areas, asset portfolios, functional requirements and organizational activity) are outside the scope of this document. This part of ISO 12006 does not provide the content of the tables, though it does give examples.