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SN EN 12006-2+A1:2009

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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

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  • Dokumenttyp: EN
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  • ICS: 11.040.40
  • Herausgeber: SNV
  • Lieferant: SNV
  • Nationales Komitee: INB/NK 129

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