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1 Scope This document provides recommendations and requirements on the handling, storage, processing and documentation of venous whole blood specimens intended for circulating cell free DNA (ccfDNA) examination during the pre-examination phase before an analytical test is performed. This document covers specimens collected in venous whole blood collection tubes. This document is applicable to…

The following deviations are intended to meet Canadian product requirements and to align with the Canadian Electrical Code, Part I. International Standard IEC 61010-2-101:2015 (second edition) forms the basis for CAN/CSA-C22.2 No. 61010-2-101, which contains the following deviations in addition to those shown in CAN/CSA-C22.2 No. 61010-1:12. Les exigences propres au Canada qui suivent…

1 Scope This document gives guidelines on the handling, storage, processing and documentation of venous whole blood specimens intended for cellular RNA examination during the pre-examination phase before a molecular examination is performed. This document covers specimens collected in venous whole blood collection tubes. This document is applicable to any molecular in vitro diagnostic…

1 Scope This document gives guidelines on the handling, storage, processing and documentation of venous whole blood specimens intended for genomic DNA examination during the pre-examination phase before a molecular examination is performed. This document covers specimens collected in venous whole blood collection tubes. This document is applicable to any molecular in vitro diagnostic…

1 Scope and object This clause of Part 1 is applicable, except as follows: 1.1.1 Equipment included in scope Replacement: Replace the text with the following: This part of IEC 61010 specifies particular safety requirements for CABINET X-RAY SYSTEMS. A CABINET X-RAY SYSTEM is a system that contains an X-ray tube installed in a cabinet which, independently of existing architectural…

This National Standard of Canada is equivalent to International Standard CEI/IEC 61010-2-040:2005. 1 Scope and object This clause of Part 1 is applicable except as follows: 1.1.1 Equipment included in scope Replacement: This International Standard specifies safety requirements for electrical equipment intended for sterilization, washing, and disinfection of medical materials in the medical,…

1 Scope and object This clause of Part 1 is applicable except as follows: 1.1.1 Equipment included in scope Replace the existing text with the following: This part of IEC 61010 specifies safety requirements for hand-held multimeters for domestic and professional use, capable of measuring MAINS. Hand-held multimeters are multi-range multifunction measuring instruments intended to measure…

1 Scope and object This clause of Part 1 is applicable except as follows: 1.1.1 Equipment included in scope Replacement: Replace the existing text with the following: This part of IEC 61010 specifies safety requirements for METERS. The METERS that have a primary purpose of measuring voltage on a live MAINS CIRCUIT are within the scope of this standard. They have various names, but all of…

1 Scope This document specifies procedures and test methods used to demonstrate the cleaning efficacy of washer-disinfectors (WD) and their accessories intended to be used for cleaning of reusable medical devices. NOTE 1 The requirements can be used for washer-disinfectors intended for use with other articles used in the context of medical, dental, laboratory, pharmaceutical and veterinary…

This National Standard of Canada is equivalent to International Standard ISO 12117:1997. 1 Scope This International Standard establishes a consistent and reproducible means of evaluating the load-carrying characteristics of tip-over protective structures (TOPS) under static loading, and prescribes performance requirements of a representative specimen under such loading. It applies to TOPS…