Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 1: Heart valve substitutes

This standard specifies particular requirements for heart valve substitutes.           This European Standard is not applicable to heart valve substitutes composed in whole, or in part, of human tissue.           With regard to safety, it gives requirements for intended performance, design attributes, materials, design evaluation, manufacturing, sterilization, packaging and information supplied by the manufacturer.           This European Standard specifies a number of test methods and requirements regarding the performance characteristics of equipment to be used to determine the physical, biological and chemical properties of heart valve substitutes and of the materials and components of which they are made.           Recommendations are also made for in vivo testing and clinical evaluation, and for the reporting of results of all types of testing and evaluation covered in this European Standard. These recommendations do not purport to comprise a complete test programme (see annex F for rationale).

Nichtaktive chirurgische Implantate - Besondere Anforderungen für Herz- und Gefäßimplantate - Teil 1: Herzklappenprothesen

Diese Norm legt besondere Anforderungen für Herzklappenprothesen fest. Diese Europäische Norm gilt nicht für Herzklappenprothesen, die vollständig oder teilweise aus menschlischem Gewebe bestehen. Im Hinblick auf die Sicherheit nennt sie Anforderungen für die vorgesehene Funktion, Konstruktions-merkmale, Werkstoffe, Bewertung der Konstruktion, Herstellung, Sterilisation, Verpackung und vom Hersteller zu liefernde Informationen.

Implants chirurgicaux non actifs - Exigences particulieres pour les implants cardio-vasculaires - Partie 1: Protheses valvulaires cardiaques

La présente norme européenne spécifie les exigences particulieres relatives aux protheses valvulaires cardiaques. La présente norme européenne ne s'applique pas aux protheses valvulaires cardiaques constituées entierement, ou en partie, de tissu d'origine humaine. En ce qui concerne la sécurité, elle présente les exigences relatives aux performances prévues, a la conception, aux matériaux, a l'évaluation de la conception, a la fabrication, a la stérilisation, a l'emballage et aux informations fournies par le fabricant.

Neaktivni kirurški vsadki (implantati) – Posebne zahteve za srčnožilne vsadke (kardiovaskularne implantate) – 1. del: Nadomestki srčne zaklopke

General Information

Status
Withdrawn
Publication Date
30-Jun-2000
Withdrawal Date
31-Mar-2006
Technical Committee
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
01-Apr-2006
Due Date
01-Apr-2006
Completion Date
01-Apr-2006

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Standards Content (Sample)

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Nichtaktive chirurgische Implantate - Besondere Anforderungen für Herz- und Gefäßimplantate - Teil 1: HerzklappenprothesenImplants chirurgicaux non actifs - Exigences particulieres pour les implants cardio-vasculaires - Partie 1: Protheses valvulaires cardiaquesNon active surgical implants - Particular requirements for cardiac and vascular implants - Part 1: Heart valve substitutes11.040.40Implantanti za kirurgijo, protetiko in ortetikoImplants for surgery, prosthetics and orthoticsICS:Ta slovenski standard je istoveten z:EN 12006-1:1999SIST EN 12006-1:2000en01-julij-2000SIST EN 12006-1:2000SLOVENSKI
STANDARD



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST EN 12006-1:2000



SIST E
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