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SSH EN 12006-2: 1998+A1:2009

Implantet kirurgjikale joaktive - Kërkesa të veçanta për implantet kardio-vaskulare - Kërkesa të veçanta për implantet kardiake dhe vaskulare - Pjesa 2: Protezat vaskulare përfshirë edhe tubat me valvul

Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits
22 dhj 2009

General information

60.60     22 dhj 2009

DPS

DPS/KT 316

European Norm

11.040.40  

anglisht  

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Scope

This standard describes specific requirements for vascular prostheses, including cardiac valve conduits, of synthetic or biological origin intended to replace, to reconstruct, to bypass or to form shunts between segments of the cardio-vascular system in humans.
This European Standard is not applicable to prostheses derived from host tissue (autografts).
NOTE A valve conduit is regarded as a composite prosthesis and falls within the scope of this standard.
With regard to safety it gives in addition to EN ISO 14630:1997, requirements for intended performance, design attributes, materials, design evaluation, manufacturing, sterilization, packaging and information supplied by the manufacturer.
This European Standard specifies the designation of materials of the manufacturer and the construction of the device, and the designation of sizes and dimensions of vascular prostheses. It specifies biological requirements for the materials of construction and for the finished product by references to appropriate International and European Standards.
In addition this European Standard specifies the designation of mechanical properties. It describes methods for the measurement and verification of the dimensions and mechanical properties stated by the manufacturer, including durability testing.
This standard also gives requirements for packaging and labelling. It provides definitions of the terms in common use.
This European Standard does not specify all possible performance or dimensional characteristics. In such cases, the European Standard does however include methods to verify the nominal values stated by the manufacturer.

Related directives

Directives related to this standards.

93/42/EEC

Pajisje Mjekësore

Të harmonizuara
2007/47/EC

Direktiva 2007/47/EC e Parlamentit Europian dhe e Këshillit të 5 shtator 2007 amendon Direktivën e Këshillit 90/385/EEC mbi përafrimin e ligjeve të Shteteve Anëtare në lidhje me pajisje medicinale aktive transplatuese, Direktiva e Këshillit 93/42/EEC në lidhje me pajisjet mjekësore dhe Direktivën 98/8/EC në lidhje me vendosjen e produkteve biocide në treg

Të harmonizuara

Life cycle

PREVIOUSLY

Replaces
SSH EN 12006-2:2000

NOW

PUBLISHED
SSH EN 12006-2: 1998+A1:2009
60.60 Standard published
22 dhj 2009

Related project

Adopted from EN 12006-2:1998+A1:2009

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