DS/EN ISO 5840-1:2015 (Valid to: 31-08-2021)

Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements

Valid to: 31-08-2021
Replaced by:
Price from:
€ 104.76


This part of ISO 5840 is applicable to heart valve substitutes intended for human implantation and provides general requirements. Subsequent parts of the ISO 5840–series provide specific requirements.
This part of ISO 5840 is applicable to both newly developed and modified heart valve substitutes and to the accessories, packaging, and labelling required for their implantation and for determining the appropriate size of the heart valve substitute to be implanted.
This part of ISO 5840 outlines an approach for qualifying the design and manufacture of a heart valve substitute through risk management. The selection of appropriate qualification tests and methods are derived from the risk assessment. The tests may include those to assess the physical, chemical, biological, and mechanical properties of heart valve substitutes and of their materials and components. The tests may also include those for preclinical in vivo evaluation and clinical evaluation of the finished heart valve substitute.
This part of ISO 5840 defines operational conditions for heart valve substitutes.
This part of ISO 5840 excludes homografts.
NOTE – A rationale for the provisions of this part of ISO 5840 is given in Annex A.

Number of pages: 70

Published: 2015-12-03

Date of approval: 2015-11-17

International relationships : EN ISO 5840-1:2015 IDT ISO 5840-1:2015 IDT

ICS: 11.040.40 - Implants for surgery, prosthetics and orthotics

Item number: M285807

*Expected revoked date: 31-08-2021



  • CEN/TC 285
  • ISO/TC 150/SC 2
  • ISO/TC 150/SC 2/WG 1

Danish committee