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…
Care quality for older persons at home and in care facilities
This document would specify requirements and recommendations for the provision of health and social care services for older persons provided by healthcare and social care personnel, irrespective of whether the service is provided in the persons own home or in a care home. The services concerned also include those offered to older people who do not reside permanently at a care home, such as…
Information technology — High efficiency coding and media delivery in heterogeneous environments — P...
This document specifies technology that supports the efficient transmission of immersive audio signals and flexible rendering for the playback of immersive audio in a wide variety of listening scenarios. These include home theatre setups with 3D loudspeaker configurations, 22.2 loudspeaker systems, automotive entertainment systems and playback over headphones connected to a tablet or smartphone.
Information technology — Cross jurisdictional and societal aspects of implementation of biometric te...
This document provides guidance on the specific considerations that need to be given when using
biometrics for major incident response. The following aspects are included within the scope of this
document:
• managing people and their identities (living or deceased) to co-ordinate the emergency response
effort
• linking reported missing persons to unidentified victims, reuniting relatives and…
Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential per...
This document is applicable to the basic safety and essential performance of oxygen conserving equipment, hereafter referred to as ME equipment, in combination with its accessories intended to conserve supplemental oxygen by delivering gas intermittently and synchronized with the patient's inspiratory cycle, when used in the home healthcare environment. Oxygen conserving equipment is…
Cybersecurity — IoT security and privacy — Cybersecurity labelling framework for consumer IoT
This document defines a Universal Cybersecurity Labelling Framework for the development and implementation of cybersecurity labelling programmes for consumer IoT products and includes guidance on the following topics:
• Risks and threats associated with consumer IoT products;
• Stakeholders, roles and responsibilities;
• Relevant standards and guidance documents;
• Conformity assessment options…
Medical electrical equipment — Part 2-69: Particular requirements for the basic safety and essential...
This document specifies requirements for the basic safety and essential performance of an oxygen concentrator in combination with its accessories, hereafter referred to as ME equipment, intended to increase the oxygen concentration of gas intended to be delivered to a single patient. Such oxygen concentrators are typically intended for use in the home healthcare environment by a single patient in…
Medical electrical equipment — Part 2-70: Particular requirements for basic safety and essential per...
This document is applicable to the basic safety and essential performance of sleep apnoea breathing therapy equipment, hereafter referred to as ME equipment, intended to alleviate the symptoms of patients who suffer from obstructive sleep apnoea by delivering a therapeutic breathing pressure to the respiratory tract of the patient. Sleep apnoea breathing therapy equipment is intended for use in…
This document specifies the requirements and test methods for external tooth bleaching products. These products are intended for use in the oral cavity, either by professional application (in-office tooth bleaching products) or consumer application (professional or non-professional home use of tooth bleaching products), or both. It also specifies requirements for their packaging, labelling and…
Transportable liquid oxygen systems for medical use — Part 2: Particular requirements for portable u...
This document specifies requirements for portable units which are part of a transportable liquid oxygen system. These are used as a supply source for oxygen therapy in home-care and in health-care facilities.
Portable units are intended to be carried by patients whilst moving around and during their off-site activities and can be refilled from a base unit through a transfilling connector.…