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Scope 1.1 These requirements apply to ultraviolet germicidal irradiation (UVGI) equipment and systems intended for installation and use in accordance with the U.S. National Electrical Code (NEC), NFPA 70 and in accordance with the Canadian Electrical Code, Part I (CEC), CSA C22.1. These requirements cover: a) UV Germicidal Equipment – These devices emit uncontained UV energy into the…

1 Scope and object 1.1 Scope 1.1.1 Equipment included in scope [Add the following] This Standard applies to the above-noted equipment that is intended to be installed or used in accordance with CSA C22.1, Canadian Electrical Code, Part I. General requirements applicable to the above-noted equipment are provided in CSA C22.2 No. 0. 1.1.2 Equipment excluded from scope [Replace NOTE 1 with…

Applies to the installation and testing of Class I and Ii biological containment cabinets. Such cabinets are designed to control and eliminate particulates and aerosols generated by routine laboratory manipulations.

Scope 1.1 This Standard applies to the use of medical devices and systems for the application of electrosurgical energy. It applies to all procedures in all health care settings where such medical devices and systems are used, including, but not limited to, the following: a) surgical facilities; b) dental clinics; c) medical offices; d) veterinary facilities; e) laboratories and other…

1 Scope 1.1 This Standard specifies requirements for the management of low- and intermediate-level radioactive waste in solid, liquid, or gaseous states. 1.2 This Standard applies to organizations and facilities that generate, possess, manage, and transport lowand intermediate-level radioactive waste, including power reactors, research institutes, laboratories, and industrial facilities…

1 Scope This document provides practical guidance for the estimation and expression of the measurement uncertainty (MU) of quantitative measurand values produced by medical laboratories. Quantitative measurand values produced near the medical decision threshold by point-of-care testing systems are also included in this scope. This document also applies to the estimation of MU for results…

1. Scope and Purpose 1.1 Scope 1.1.1 This Standard applies to packaged heat/energy-recovery ventilators (HRV/ERV) that comprise factory-assembled elements including fans or blowers, in which heat or heat and moisture is transferred between two isolated airstreams. 1.1.2 This Standard specifies laboratory methods of testing and procedures for rating the apparent effectiveness and…

This National Standard of Canada is based on International Standard IEC 1010-2-020:1992. 1. Scope and Object This clause of Part 1 is applicable except as follows: 1.1 Scope This Particular Standard specifies requirements for the safety of electrically powered laboratory centrifuges designed to be installed and used in accordance with the Rules of the Canadian Electr ical Code,…

This National Standard of Canada is based on International Standard IEC 61010-1:2001, and is common with UL 61010-1. 1 Scope and object 1.1 Scope 1.1.1 Equipment included in scope This part of IEC 61010 specifies general safety requirements for electrical equipment intended for professional, industrial process, and educational use, any of which may incorporate computing devices, as defined in…

1 Scope 1.1 Requirements for operation and maintenance of HCFs This Standard describes the requirements, including quality system requirements, for the O&M of an HCF. It sets out specific requirements for a) facility architectural systems; b) exterior site elements related to the building and its functions; c) utilities; d) the facility’s infrastructure, including, but not limited…