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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Cardiovascular implants – Endovascular devices – Part 3: About Us Info center Standardization.

Endovascular prostheses ISO Monday to Friday – 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 valve component of valved conduits constructed with an endovascular prosthesis component and the combination izo 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. This document can be helpful in identifying the appropriate evaluation of the endovascular prosthesis component of a valved 25539–1, 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. Cardiovascular implants – Endovascular devices – Part 2: Du abonnerer allerede dette emne.

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

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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Similarly, 255539-1 prosthesis configurations e. To find similar documents by classification: 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 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. Please contact the ISRM info center. Certified by ISO Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in 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.

This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. Forkert brugernavn eller adgangskode. Vis ikke denne igen. This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants.

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 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.

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Prices subject to change without notice. Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e. Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses.

Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. The following bibliographic 25539-11 is provided to assist you with your purchasing decision: 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.

ISO 25539-1:2017

Vena cava filters 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. Related international standards This standard is identical to: 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 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.