ISO 25539 PDF

Part 1: Endovascular prostheses. Implants cardiovasculaires — Dispositifs endovasculaires —. Partie 1: Prothèses endovasculaires. STANDARD. ISO. ISO Cardiovascular implants—. Endovascular devices—Part 1: Endovascular prostheses. American. National. Standard. PREVIEW COPY. ISO /. A/. (R) Cardiovascular implants —. Endovascular devices —. Part 1: Endovascular prostheses —. Amendment 1: Test methods.

Author: Dulkis Vudosho
Country: Denmark
Language: English (Spanish)
Genre: Life
Published (Last): 18 November 2007
Pages: 480
PDF File Size: 17.81 Mb
ePub File Size: 7.79 Mb
ISBN: 670-6-66614-279-5
Downloads: 15057
Price: Free* [*Free Regsitration Required]
Uploader: Kazahn

This document can be helpful in identifying the appropriate evaluation of the endovascular prosthesis component of a valved conduit, but specific requirements and testing are not described for these devices.

This document can be considered as a supplement to ISOwhich specifies general requirements for lso performance of non-active surgical implants.

Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. The valve component of valved conduits constructed with an endovascular prosthesis component and the combination of the valved component and the endovascular prosthesis component are excluded from the scope of this document.

Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e. Guidance for the development of in vitro test methods is included in an informative annex to this document. Balloons used to achieve adequate apposition of the prosthesis with the vessel wall or overlapping components are within the scope of this document, even if they are not integral to the endovascular system.

Monday to Friday – Kontakt venligst Dansk Standard. Balloons used to achieve adequate apposition of the prosthesis with the vessel wall or overlapping components are within the scope of this document, even if they are not integral to the endovascular system. The requirements for, and the evaluation of, degradation and other time-dependant aspects of absorbable materials used in the construction of endovascular prostheses are not addressed in this document.

  KLV 24EX430 MANUAL PDF

Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. Although contra-lateral iliac artery occluders when used as an integral part of aorto-uni-iliac endovascular prosthesis are within the scope of this document, specific requirements and testing are not described for these devices.

Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. Similarly, specific prosthesis configurations e. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. Guidance for the development of in vitro test methods is included in an informative iiso to this document.

BS EN ISO 25539-1:2009

The valve component of valved conduits constructed with an endovascular prosthesis component and the combination of the valved component and the endovascular prosthesis component isp excluded from the scope of this document. Final text received or FDIS registered for formal approval. Similarly, specific prosthesis configurations e. The requirements for, and the evaluation of, degradation and other time-dependant aspects of absorbable materials used in the construction of endovascular prostheses are not addressed in this document.

Forkert brugernavn eller adgangskode. Proof sent to secretariat or Iwo ballot initiated: Guidance for the development of in vitro test methods is included in an informative annex to this document. Check out our FAQs.

Vis ikke denne igen. Life cycle A standard is reviewed every 5 years 00 Preliminary. This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. The valve component of valved conduits constructed with an endovascular prosthesis component and the combination of the valved component and the endovascular prosthesis component are excluded from 255399 scope of this document.

  FIBRE BUNDLES HUSEMOLLER PDF

BS EN ISO – Cardiovascular Implants. Endovascular devices. Endovascular prostheses

Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e. Although contra-lateral iliac artery occluders when used as an integral part of aorto-uni-iliac endovascular prosthesis are within the scope of this document, specific requirements and testing are not described for these kso.

Balloons used to achieve adequate apposition of the prosthesis with the vessel wall or overlapping components are within the scope of this document, even if they are not integral to the endovascular system.

Although uses of iiso systems other than treatment of arterial aneurysms or stenoses e. This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants.

Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses.

Radial Force ISO

This document can be helpful in oso the appropriate evaluation of the endovascular prosthesis component of a valved conduit, but specific requirements and testing are not described for these devices. Although contra-lateral iliac artery occluders when used as an integral part of aorto-uni-iliac endovascular prosthesis are within the scope of this document, specific requirements and testing are not described for these devices.

Cardiovascular implants – Endovascular devices – Part 1: The requirements for, and the evaluation of, degradation and other time-dependant aspects of absorbable materials used in the construction of endovascular prostheses are not addressed in this document.