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1 Scope 1.1 This Standard deals with the following subjects: a) the use of electrical surgical units (ESUs) — medical devices and systems for the application of electrosurgical energy; b) training for the use of ESUs; and c) the installation of ESUs in any health care facility (HCF), as defined in Clause 3. 1.2 This Standard provides requirements for the education, training, purchasing,…

1 Scope 1.1 Except as indicated in Clause 1.2, Part 1 of this Standard applies to all boilers, pressure vessels, pressure piping, and fittings, as provided for by the Act (as defined in Clause 3) and identified in Part 1 of this Standard. Notes: 1) It is possible that the size limitations specified in provincial or territorial statutes or regulations will differ from those specified in Part…

1 Scope 1.1 General This Standard specifies requirements for the design, manufacture, construction, modification, operation, inspection, testing, and maintenance of passenger ropeways and passenger conveyors. Requirements for abnormal or unusual conditions are not specifically provided for, nor are all details of engineering and construction prescribed. It is intended that all work performed…

This document specifies the information accompanying geosynthetics to enable the user on site to identify the goods as being identical to the goods ordered. The positive identification, e.g. of unwrapped or rolled-out geosynthetics, is an important aim of this document. The information specified does not replace a technical data sheet and cannot be used to verify the conformance of the product…

1.1 General This document is the base standard for a number of other standards dealing with water treatment equipment, water, dialysis water, concentrates, and dialysis fluid (ISO 23500 series) and provides dialysis practitioners with guidance on the preparation of dialysis fluid for haemodialysis and related therapies and substitution fluid for use in online therapies, such as…

This document specifies minimum requirements for concentrates used for haemodialysis and related therapies. This document is addressed to the manufacturer of such concentrates. In several instances in this document, the dialysis fluid is addressed, which is made by the end user, to help clarify the requirements for manufacturing concentrates. Because the manufacturer of the concentrate does not…

This document defines the conceptual schema for spatial references based on geographic identifiers. It establishes a general model for spatial referencing using geographic identifiers and defines the components of a spatial reference system. It also specifies a conceptual scheme for a gazetteer. Spatial referencing by coordinates is addressed in ISO 19111. However, a mechanism for recording…

The ISO 11929 series specifies a procedure, in the field of ionizing radiation metrology, for the calculation of the "decision threshold", the "detection limit" and the "limits of the coverage interval" for a non-negative ionizing radiation measurand when counting measurements with preselection of time or counts are carried out. The measurand results from a gross…

The ISO 11929 series specifies a procedure, in the field of ionizing radiation metrology, for the calculation of the "decision threshold", the "detection limit" and the "limits of the coverage interval" for a non-negative ionizing radiation measurand when counting measurements with preselection of time or counts are carried out. The measurand results from a gross…

The ISO 11929 series specifies a procedure, in the field of ionizing radiation metrology, for the calculation of the "decision threshold", the "detection limit" and the "limits of the coverage interval" for a non-negative ionizing radiation measurand when counting measurements with preselection of time or counts are carried out. The measurand results from a gross…