ISO 25539-1 PDF

Reference number. ISO (E). This is a preview of “ISO “. Click here to purchase the full version from the ANSI store. Buy I.S. EN ISO CARDIOVASCULAR IMPLANTS – ENDOVASCULAR DEVICES – PART 1: ENDOVASCULAR PROSTHESES. Buy AAMI ISO Cardiovascular Implants – Endovascular Devices – Part 1: Endovascular Prostheses from SAI Global.

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This document is available in either Paper or PDF format. Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. Vascular stents ISO 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 kso scope of this document, specific requirements and testing are not described for these devices.

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Dauerhaftigkeitsprüfung an endovaskulären Prothesen nach ISO

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.

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 the scope of this document.

First Balkan IT Conference for business platform for standardization Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses.

Prices subject to change without notice. Final text received or FDIS registered for formal approval. Life cycle A standard is reviewed every 5 years 00 Preliminary. To find similar documents by classification: 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.

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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.

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.

This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document.

Similarly, specific prosthesis configurations e.

BS EN ISO 25539-1:2009

Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e. Kontakt venligst Dansk Standard. This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. Although uses of endovascular systems other than treatment 255339-1 arterial aneurysms or stenoses 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. 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. Although contra-lateral iliac artery occluders when 25539–1 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.

Document Number ISO 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.

Balloons used to achieve adequate apposition of the prosthesis with the vessel wall or overlapping components are within 255399-1 scope of this document, even if they are not integral to the endovascular system.

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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 ios 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. Endovascular prostheses ISO 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.

Cardiovascular implants – Endovascular devices – Part 3: My account Shoping cart 0 Help. This document can be helpful isl identifying the appropriate evaluation of the endovascular prosthesis component of a valved conduit, but specific requirements and testing are not described 255339-1 these devices. Please contact the ISRM info center. Vena cava filters ISO Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. Guidance for the development of in vitro test methods is included in an informative annex to this document.

The following bibliographic material is provided to assist you ios your purchasing decision: FAQ What is standard Become a member? This document can be helpful in identifying the appropriate evaluation of the endovascular prosthesis oso of a valved conduit, but specific requirements and testing are not described for these devices. 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.