DIN EN 14299 E : 2004

Foreword<br>Introduction<br>1 Scope<br>2 Normative references<br>3 Terms and definitions<br>4 Intended performance<br>5 Design attributes<br>6 Materials<br>7 Design evaluation<br>8 Manufacturing<br>9 Sterilization<br>10 Packaging<br>11 Information supplied by the manufacturer<br>Annex A (informative) Cross reference of specific aims<br>Annex B (informative) Definitions of reportable clinical<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;events<br>Annex ZA (informative) Clauses of this European Standard<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;addressing essential requirements or<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;other provisions of EU Directives<br>Bibliography

Defines requirements for arterial stents and endovascular prostheses and their deployment intended to correct or compensate for a defect of an artery.