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ISO 22442-1:2015 applies to medical devices other than in vitro diagnostic medical devices manufactured utilizing materials of animal origin, which are non-viable or have been rendered non-viable. It specifies, in conjunction with ISO 14971, a procedure to identify the hazards and hazardous situations associated with such devices, to estimate and evaluate the resulting risks, to control these…

ISO 22442-2:2015 specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical devices utilizing materials of animal origin other than in vitro diagnostic medical devices. It applies where required by the risk management process as described in ISO 22442‑1. NOTE 1 Selective sourcing…

1.1 This Standard specifies requirements for occupational apparel that is a) capable of signalling the user’s presence visually; and b) intended to provide the user with conspicuity in hazardous situations under any light conditions and under illumination by vehicle headlights. 1.2 Performance requirements are included for colour, retroreflection, and minimum areas, as well as for the…

1.1 This Standard specifies requirements for polyethylene of raised temperature (PE-RT) tubing systems that are comprised of tubing and fittings. Tubing covered by this Standard is made in Standard Dimensional Ratio 9 (SDR 9). Systems are pressure rated at two temperatures: 1105 kPa at 23 °C and 690 kPa at 82 °C. Systems are intended for use in potable water distribution systems or other…

1 Scope and object [In the eighth paragraph, replace “IEC 62115” with “CSA C22.2 No. 149”] [Add the following paragraph at the end of the clause] This Standard covers the above-noted products that are intended to be installed or used in accordance with CSA C22.1, Canadian Electrical Code, Part I. 1 Domaine d'application et objet [Dans le huitième paragraphe, remplacer «IEC 62115» par «CSA…

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 by the following: This part of IEC 61010 applies to automatic and semi-automatic laboratory equipment for analysis and other purposes. Automatic and semi-automatic laboratory equipment consists of instruments or systems for measuring or modifying one or…

1.1 This Standard specifies a) energy performance requirements for factory-made, self-contained, electrically-operated, mechanically-refrigerated household dehumidifiers with daily water-removal capacities of up to 87.5 L (185 U.S. pints); b) test procedures for measuring capacity, standby power, off mode power, and active mode energy use; and c) minimum and high efficiency energy factor, EF. 1.2…

This Standard covers medical electrical equipment that is intended to be installed or used in accordance with CSA C22.1, Canadian Electrical Code, Part I. [Add the following note] Note 1A: Attention should be directed to the recommendations for patient monitoring during anaesthesia made by national, professional, and regulatory bodies. These recommendations include, but are not limited to,…

1.1 This Standard applies to cord-connected microwave ovens intended for use on nominal 120/240 V branch circuits and microwave ovens intended for permanent connection to branch circuits up to 240 V, manufactured for use in homes and similar locations 1.2 This Standard specifies methods of testing the energy consumption in both active and standby modes of electrically operated microwave…

1.1 This Standard specifies methods for measuring the volume, energy consumption, and total display area (TDA) of electrically operated commercial refrigeration equipment. 1.2 This Standard applies to commercial refrigerator, refrigerator-freezer, and freezer cabinets and merchandisers that are intended for displaying, storing, or holding food products including canned and bottled beverages…