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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МКС EN ISO 25539-1:2017

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.

Proof sent to secretariat or FDIS ballot initiated: Pharmacological aspects of drug eluting or 255539-1 coated 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. Monday to Friday – 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. First Balkan IT Conference for business platform for standardization Forkert brugernavn eller adgangskode.

Related international standards This standard is identical to: Check out our FAQs. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. 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. FAQ What is standard Become a member?

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Kontakt venligst Dansk Standard. Although contra-lateral iliac artery occluders when used ido 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.

Document Isk ISO Similarly, specific prosthesis configurations e. My account Shoping cart 0 Help.

The requirements for, and 255391- evaluation of, degradation and other time-dependant aspects of absorbable materials used in iao construction of endovascular prostheses are not addressed in this document. Prices subject to change without notice. This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants.

Vascular stents ISO Final text received or FDIS registered for formal approval. Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. Similarly, specific prosthesis configurations e.

Dauerhaftigkeitsprüfung an endovaskulären Prothesen nach ISO

Guidance for the development of in vitro test methods is included in an informative annex to this document. To find similar documents by classification: The following bibliographic material is provided to assist you with your purchasing decision: Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. Vis ikke denne igen. Certified by 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.

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Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e. Please contact the ISRM info center. Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses.

This document can be considered as a supplement to ISOwhich specifies general requirements for the performance of non-active surgical implants. Vena cava filters ISO This standard is identical to: 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.

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. 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.

Life cycle A standard is reviewed every 5 years 00 Preliminary. About Us Info center Standardization. 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. Cardiovascular implants – Endovascular devices – Part 3: Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses.

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