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English: These Regulations contain the legislative measures necessary for the implementation of three European Community Directives- Council Directive 90-385-EEC on the approximation of the laws of the Member States relating to active implantable medical devices, as amended; Council Directive 93-42-EEC concerning medical devices, as amended; and Directive 98-79-EC of the European Parliament ...
The general standard IEC 60601-1 – Medical electrical equipment – Part 1: General requirements for basic safety and essential performance – gives general requirements of the series of standards. 60601 is a widely accepted benchmark for medical electrical equipment and compliance with IEC60601-1 has become a requirement for the commercialisation of electrical medical equipment in many ...
The Standard "ISO/IEEE International Standard - Health informatics--Point-of-care medical device communication - Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication" [9] is derived from the IEEE 11073-10201 Domain Information Model. It is designed to meet the requirements of networked ...
An urgent care center (UCC), also known as an urgent treatment centre (UTC) in the United Kingdom, is a type of walk-in clinic focused on the delivery of urgent ambulatory care in a dedicated medical facility outside of a traditional emergency department located within a hospital.
One of London Ambulance Service's frontline vehicles The London Air Ambulance in action Peugeot Ambulance of the Scottish Ambulance Service. Emergency medical services in the United Kingdom provide emergency care to people with acute illness or injury and are predominantly provided free at the point of use by the four National Health Services (NHS) of England, Scotland, Wales, and Northern ...
ISO 15223 Medical devices – Symbols to be used with medical device labels, labelling, and information to be supplied ISO 15223-1:2016 Part 1: General requirements; ISO 15223-2:2010 Part 2: Symbol development, selection and validation; ISO 15225:2016 Medical devices – Quality management – Medical device nomenclature data structure
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National Institute for Biological Standards and Control – responsible for the standardisation and control of biological medicines; The MHRA has several independent advisory committees which provide the UK Government with information and guidance on the regulation of medicines and medical devices.