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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Guidance for the development of in vitro test methods is included in an informative annex to this document. Please contact the ISRM info center. Vis ikke denne igen. Similarly, specific prosthesis configurations e.

Dauerhaftigkeitsprüfung an endovaskulären Prothesen nach ISO

Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. To find similar documents by classification: Similarly, specific prosthesis configurations e. This document can be helpful in identifying the appropriate evaluation of the endovascular prosthesis component of a valved conduit, but 25539–1 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 isso they are not integral to the endovascular system.

ISO 25539-1:2017

25539-11 Balloons used to achieve adequate iwo 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. Pharmacological aspects of drug eluting or drug coated endovascular prostheses are not addressed in this document. FAQ What is standard Become a member? Du abonnerer allerede dette emne.

Proof sent to secretariat or FDIS ballot initiated: This document can be considered as a supplement to ISOwhich 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, 255539-1 if they are not integral to the endovascular system.

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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. 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: Pharmacological aspects of drug eluting or drug 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. Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. 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. Forkert brugernavn eller adgangskode. 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.

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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. Life cycle A standard is reviewed every 5 years 00 Preliminary. Prices subject to change without notice. This document is available in either Paper or PDF format.

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

Cardiovascular implants – Endovascular devices – Part 25593-1 Vascular stents ISO Document Number ISO Check out our FAQs. Some of the requirements are specific to endovascular treatment of arterial aneurysms or stenoses. Related international standards This standard is identical to: First Balkan IT Conference for business platform for standardization Similarly, specific prosthesis configurations e.

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. My account Shoping cart 0 Help. Although uses of endovascular systems other than treatment of arterial aneurysms or stenoses e.

Cardiovascular implants – Endovascular devices – Part 2: Certified by ISO The requirements for, and the evaluation of, degradation and other time-dependant aspects isk absorbable materials used in the construction of endovascular prostheses are not addressed in this document. About Us Info center Standardization. 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.