ENV 12018:1997

ENV 12018:1997 is a standardization document published by the European Committee for Standardization (CEN). Its full title is "Identification, administrative, and common clinical data structure for Intermittently Connected Devices used in healthcare (including machine readable cards)". This standard covers: This European Prestandard establishes a common framework for the content and the structure of identification, administrative and common clinical data. It applies exclusively to situations in which such data are recorded on or transported by Intermittently Connected Devices (ICDs) which are intended for use in healthcare. This European Prestandard specifies the basic structure of the data, but does not specify particular data-sets for storage on devices.

This European Prestandard establishes a common framework for the content and the structure of identification, administrative and common clinical data. It applies exclusively to situations in which such data are recorded on or transported by Intermittently Connected Devices (ICDs) which are intended for use in healthcare. This European Prestandard specifies the basic structure of the data, but does not specify particular data-sets for storage on devices.

ENV 12018:1997 is classified under the following ICS (International Classification for Standards) categories: 11.020 - Medical sciences and health care facilities in general; 35.240.60 - IT applications in transport. The ICS classification helps identify the subject area and facilitates finding related standards.

ENV 12018:1997 has the following relationships with other standards: It is inter standard links to EN ISO 3248:2000, CR 14302:2002, EN 1359:1998, EN 858-1:2002, EN 1825-1:2004, EN ISO 8130-8:2010. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

ENV 12018:1997 is associated with the following European legislation: Standardization Mandates: M/255. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.

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