ISO/TS 17137:2014

Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants

Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants

Digital Document2014 edition2014Purchase Options

Referenced standards

ASTM F1635-11ASTM F1980-07ASTM F2052-06ASTM F2119-07ASTM F2129-08ASTM F2182-11aASTM F2213-06ASTM F2394-07ASTM F2503-08ASTM F2743-11ASTM F2902-12ASTM F2914-12ISO/IEC Guide 51:1999
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ISO/TS 17137:2014

Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants

Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants

ISO/TS 17137:2014 outlines design verification and validation considerations for absorbable cardiovascular implants.

ISO/TS 17137:2014 is applicable to implants in direct contact with the cardiovascular system, where the intended action is upon the circulatory system. ISO/TS 17137:2014 does not address the specific evaluation of issues associated with viable tissues, viable cells, and/or implants with non-viable biological materials and their derivatives. Additionally, procedures and devices used prior to and following the introduction of the absorbable cardiovascular implant (e.g. balloon angioplasty devices) are excluded from the scope of ISO/TS 17137:2014 if they do not affect the absorption aspects of the implant. A cardiovascular absorbable implant may incorporate substance(s) which, if used separately, can be considered to be a medicinal product (drug product) but the action of the medicinal substance is ancillary to that of the implant and supports the primary mode of action of the implant.

Edition2014
Published Date2014
Published ByISO/TS
Page Count26