Rechercher

This document specifies requirements for the respiratory tubing and connectors used to convey respirable gases to a patient in the healthcare and homecare environments and provide a safe connection between the gas supply device and the patient interface. Respiratory tubing and connectors are mainly used for delivery of oxygen but can also be used for respirable air or oxygen/air mixtures and…

IEC 61000-2-4:2024 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition. IEC 61000-2-4:2024 is related to conducted disturbances in the frequency range from 0 kHz to 150 kHz. It gives…

This document specifies the requirements and test methods for protective gloves intended to protect the user against micro-organisms. NOTE            If other protection features are needed, e.g. chemical risks, mechanical risks, thermal risks, electrostatic dissipation etc., the appropriate specific performance standard is used in addition. Further information on protective gloves standards can…

This document specifies the requirements for protective gloves intended to protect the user against dangerous chemicals and defines terms to be used. NOTE            If other protection features are covered, e.g., mechanical risks, thermal risks, electrostatic dissipation etc., the appropriate specific performance standard is used in addition. Further information on protective gloves standards…

This document specifies the design and dimensions for two small-bore connectors intended to be used for connections in respiratory applications of medical devices and accessories. One connector (R1) is intended for use on medical devices and accessories subjected to pressures up to 15 kPa (e.g. a breathing system). The other connector (R2) is intended for use on medical devices and accessories…

This document specifies the design and dimensions for two small-bore connectors intended to be used for connections in respiratory applications of medical devices and accessories. One connector (R1) is intended for use on medical devices and accessories subjected to pressures up to 15 kPa (e.g. a breathing system). The other connector (R2) is intended for use on medical devices and accessories…

1 Scope 1.1 Inclusions This Standard specifies the requirements for distribution transformers except for those distribution transformers covered by CSA C2.2, CSA C227.3, and CSA C227.4. Note: The operation of transformers complying with this Standard by other than an electric utility might be subject to additional requirements by the electrical inspection authority having jurisdiction. 1.2…

1 Scope 1.1 The wire connectors covered by these requirements are intended for use with copper conductor in accordance with installations covered by the National Electrical Code, NFPA 70; the Canadian Electrical Code, Part I, CSA C22.1; and NOM 001 SEDE, Standard for Electrical Installations. The requirements in this standard cover twist-on style splicing sealed wire connectors intended for…

Scope Replacement: NOTE 1 There is guidance or rationale for this subclause contained in Clause AA.2. This document applies to the basic safety and essential performance of a critical care ventilator in combination with its accessories, hereafter referred to as ME equipment: ? intended for use in an environment that provides specialized care for patients whose conditions can be life-…

1 Scope 1.1 General This Standard provides core competency requirements for GSAR operations for the three core roles of searcher, team leader, and SAR manager. 1.2 Purpose This Standard was developed to provide a foundation for interoperability and portability of GSAR skills within Canada. It is intended to facilitate training curriculum development and professional development planning so…