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This International Standard has been prepared for surgically implanted heart valve substitutes with emphasis on specifying types of in vitro testing, preclinical in vivo and clinical evaluations, reporting of all in vitro, preclinical in vivo, and clinical evaluations and labeling and packaging of the device. This process is intended to clarify the required procedures prior to market release and to enable prompt identification and management of any subsequent issues. This part of ISO 5840 is to be used in conjunction with ISO 5840-1. The committee responsible for this standard is NA 027-02-17-01 UA "Herz- und Gefäßimplantate" ("Cardiovascular implants") at DIN.
This document replaces DIN EN ISO 5840:2009-08 .
This document has been replaced by: DIN EN ISO 5840-2:2016-05 .