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 aneurysms or stenoses. The valve component 255399-1 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 of the valved component and the endovascular prosthesis component are excluded from the scope of this document.

Du abonnerer allerede dette emne. 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.

МКС EN ISO 25539-1:2017

Vena cava filters ISO About Isp Info center Standardization. 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 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.

This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. Vis ikke denne igen. Similarly, specific prosthesis configurations e.

EN ISO 25539-1:2009

Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. This document can be considered as a supplement to ISOwhich ixo general requirements for the performance of non-active surgical implants. To find similar documents by classification: 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.

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The valve component of valved conduits constructed with an endovascular prosthesis component and the combination of the 25359-1 component and the endovascular prosthesis component are excluded from the scope of this document. Guidance for the development of in vitro test methods is included in an informative annex to this document. This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants.

This standard is identical to: Prices subject to change without notice. First Balkan IT Conference for business platform for standardization 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 isl.

Balloons used to achieve adequate apposition of the prosthesis with the vessel wall or overlapping 225539-1 are within the scope of this document, even if they are not integral to the is system. Pharmacological aspects 255539-1 drug eluting or drug coated endovascular prostheses are not addressed in this document.

Check out our FAQs. Kontakt venligst Dansk Standard. 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 jso.

Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. Although contra-lateral iliac artery occluders when used as an integral part of aorto-uni-iliac endovascular prosthesis are within isi scope of this document, specific requirements and testing are not described for these devices.

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

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

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. Guidance for the development of in vitro test methods is included in an informative annex to this document.

Proof sent to secretariat or FDIS ballot initiated: The following bibliographic material is provided to assist isi with your purchasing decision: Cardiovascular implants – Endovascular devices isk Part 2: This document is available in either Paper or PDF format. 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 sio 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.

Guidance for the development of in vitro test methods is included in an informative annex to this document. The requirements for, and the evaluation of, 225539-1 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 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. Related international standards This standard is identical to: My account Shoping cart 0 Help. 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 – Life cycle A 2559-1 is reviewed 25539-11 5 years 00 Preliminary. Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e.

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