ISO/TS 19218-1 was prepared by Technical Committee ISO/TC 210, Quality management and corresponding general aspects for medical devices. This first edition of ISO/TS 19218-1 , together with ISO/TS 19218-2 , cancels and replaces ISO/TS 19218:2005 , which has been technically revised.

ISO/TS 19218 WHO Informal Consultation on Nomencla Home. Support. Contact. About.

This is a Draft for Development, it is not a British Standard. It reproduces verbatim ISO/TS 19218:2005. PD ISO/TS 19218-2:2012 Medical devices. Hierarchical coding structure for adverse events Evaluation codes, Category: 03.120.10 Quality management and Amendment 1 to ISO/TS 19218 -1:2011 was prepared by Technical Committee ISO/TC 210, Quality management and corresponding general aspects for medical devices. PD ISO/TS 19218-2:2012 Medical devices.

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In accordance with Adobe's licensing policy, this file may be printed or viewed but ISO/TS 19218-1 was prepared by Technical Committee ISO/TC 210, Quality management and corresponding general aspects for medical devices. This first edition of ISO/TS 19218-1, together with ISO/TS 19218-2, cancels and replaces ISO/TS 19218:2005, which has been technically revised. ISO/TS 19218:2005 specifies requirements for a coding structure for describing adverse events related to medical devices. This code is intended for use by medical device users, manufacturers and regulatory authorities.

DS/ISO/TS 19218:2005 ( Withdrawn ) Medical devices - Coding structure for adverse event type and cause Add to cart

19199. 108,0.

ISO/TS 19218-1:2011/Amd 1:2013. Withdrawn Date published: 07/11/20

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19198. 88,9.
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ISO/TS 19218-1:2011 specifies requirements for a hierarchical coding structure for describing adverse events relating to medical devices. The codes are intended for use by medical device users, manufacturers, regulatory authorities, health care facilities and other organizations. Abstract 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. ISO/TS 19218:2005 specifies requirements for a coding structure for describing adverse events related to medical devices.

OKI Toner White - C711WT- 6K pages ISO. 5409. 44341902 19218. 97001435.
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ISO/TS 19218-2 was prepared by Technical Committee ISO/TC 210, Quality management and corresponding general aspects for medical devices. This first edition of ISO/TS 19218-2, together with ISO/TS 19218-1, cancels and replaces ISO/TS 19218:2005, which has been technically revised.

The codes are intended for use by medical device users, manufacturers, regulatory authorities, health care facilities and other organizations. 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.

20 Apr 2016 Accessed 29 March 2016. Search in Google Scholar. [10] ISO/TS 19218-1:2011 – Medical devices – Hierarchical coding structure for adverse 

The codes are intended for use by medical device users, ISO/TS 19218-2 was prepared by Technical Committee ISO/TC 210, Quality management and corresponding general aspects for medical devices. This first edition of ISO/TS 19218-2, together with ISO/TS 19218-1, cancels and replaces ISO/TS 19218:2005, which has been technically revised. ISO/TS 19218-1 was prepared by Technical Committee ISO/TC 210, Quality management and corresponding general aspects for medical devices. This first edition of ISO/TS 19218-1, together with ISO/TS 19218-2, cancels and replaces ISO/TS 19218:2005, which has been technically revised.

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