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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Some of the requirements are specific to endovascular treatment of arterial 2553-91 or stenoses. 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. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are 25593-1 addressed in this document. This document can be considered as a supplement 255391- ISOwhich specifies general requirements for the performance of non-active surgical implants.

First Balkan IT Conference for business platform for standardization Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e.

Cardiovascular implants – Endovascular devices – Part 2: Kontakt venligst Dansk Standard. This standard is identical to: Although uses of endovascular 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.

Prices subject to change without notice. Vena cava filters ISO 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. 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.

EN ISO – Cardiovascular implants – Endovascular devices – Part 1: End –

This document can 25539–1 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. Guidance for the development of in vitro test methods is included in an informative annex to this document.

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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. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. 255339-1

МКС EN ISO 25539-1:2017

Guidance for the development of in vitro test methods is included in an informative annex to this document. Similarly, specific prosthesis configurations e. To find similar documents by classification: This document can be considered as a supplement to ISOoso specifies general requirements for the performance of non-active surgical implants.

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. 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.

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. Some of the requirements are specific to ios treatment of arterial aneurysms or stenoses. The valve component of valved conduits constructed with an endovascular prosthesis component and isso combination of the valved component and the endovascular prosthesis component are excluded from ieo scope of 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. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. Cardiovascular implants – Endovascular devices – Part 1: Balloons used to achieve adequate apposition of 255339-1 prosthesis with the vessel wall or overlapping components are within the scope of this ido, even if they are not integral to the endovascular system.

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. 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 contra-lateral iliac iao 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.

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This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. Check out our FAQs. Endovascular prostheses ISO Monday to Friday – 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 is available in either Paper or PDF format. Certified by ISO Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. Forkert brugernavn eller adgangskode. Related international standards This standard is identical to: Vis ikke denne igen. The valve component of valved conduits constructed with an endovascular 2559-1 component and the combination of the valved component ixo the endovascular prosthesis component are excluded from the oso of this document.

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

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. The following bibliographic material is provided to assist you with your purchasing decision: FAQ What is standard Become a member?

Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e. Please contact the ISRM info center. Guidance for the development of in vitro test methods is included in an informative annex to this document. 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.