CSA Group Medical devices - Hierarchical coding structure for adverse events - Part 2: Evaluation codes ISO/TS 19218-2:2012

Description
ISO/TS 19218-2:2012 specifies requirements for a hierarchical coding structure for characterizing the results of the analysis or evaluation of adverse events relating to medical devices. The codes are intended primarily for use by medical device manufacturers and regulatory authorities. They can also be used for coding the results of the analysis or evaluation of events other than those related to death or serious injury, as well as malfunctions that could lead to death or serious injury. ISO/TS 19218-2:2012 is not intended to be used to decide whether or not an incident is reportable.
Description
ISO/TS 19218-2:2012 specifies requirements for a hierarchical coding structure for characterizing the results of the analysis or evaluation of adverse events relating to medical devices. The codes are intended primarily for use by medical device manufacturers and regulatory authorities. They can also be used for coding the results of the analysis or evaluation of events other than those related to death or serious injury, as well as malfunctions that could lead to death or serious injury. ISO/TS 19218-2:2012 is not intended to be used to decide whether or not an incident is reportable.

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Medical devices - Hierarchical coding structure for adverse events - Part 2: Evaluation codes - ISO/TS 19218-2:2012 - CSA Group
Toronto, Ontario, Canada
Medical devices - Hierarchical coding structure for adverse events - Part 2: Evaluation codes
ISO/TS 19218-2:2012
Medical devices - Hierarchical coding structure for adverse events - Part 2: Evaluation codes ISO/TS 19218-2:2012
ISO/TS 19218-2:2012 specifies requirements for a hierarchical coding structure for characterizing the results of the analysis or evaluation of adverse events relating to medical devices. The codes are intended primarily for use by medical device manufacturers and regulatory authorities. They can also be used for coding the results of the analysis or evaluation of events other than those related to death or serious injury, as well as malfunctions that could lead to death or serious injury. ISO/TS 19218-2:2012 is not intended to be used to decide whether or not an incident is reportable.

ISO/TS 19218-2:2012 specifies requirements for a hierarchical coding structure for characterizing the results of the analysis or evaluation of adverse events relating to medical devices. The codes are intended primarily for use by medical device manufacturers and regulatory authorities. They can also be used for coding the results of the analysis or evaluation of events other than those related to death or serious injury, as well as malfunctions that could lead to death or serious injury.

ISO/TS 19218-2:2012 is not intended to be used to decide whether or not an incident is reportable.

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Technical Specifications

  CSA Group
Product Category Standards and Technical Documents
Product Number ISO/TS 19218-2:2012
Product Name Medical devices - Hierarchical coding structure for adverse events - Part 2: Evaluation codes
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