| Standard Number | 13/30232902 DC |
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| Title | BS ISO 14708-1. Implants for surgery. Active implantable medical devices. Part 1. General requirements for safety, marking and for information to be provided by the manufacturer |
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| Status | Current, Draft for public comment |
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| Publication Date | 29 April 2013 |
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| Normative References(Required to achieve compliance to this standard) | IEC 60068-2-14:2009, IEC 60068-2-27:2008, IEC 60068-2-47:2005, IEC 60068-2-64:2008, IEC 60601-1:2005, IEC 60601-1-2:2007, IEC 62127-1:2007, IEC 62304:2006, IEC 62366:2007, ISO 10993-1:2009, ISO 11607-1:2006, ISO 14155:2011, ISO 14971:2007, ISO 8601:2004 |
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| Informative References(Provided for Information) | EN 50061:1988, EN 60068-2-64:1994, ISO 7000, ISO 11135-1, ISO 11137-1, ISO 11137-2, ISO 13485, ISO/TR 14283:2004, ISO 14937, ISO 15223-1:2102, ISO 17665-1, ISO/TS 10974, 90/385/EEC, 96/29/Eu |
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| International Relationships | ISO/DIS 14708-1:2013 |
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| Draft Expiry Date | 23 June 2013 |
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| Descriptors | Implants (surgical), Orthopaedic equipment, Alloys, Orthopaedics, Chemical composition, Tensile strength, Crystal microstructure |
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| ICS | 11.040.40
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| Committee | CH/150/2 |
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| Publisher | BSI |
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| Format | A4 |
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| Delivery | Yes |
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| Pages | 72 |
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| File Size | 997 KB |
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| Notes | Warning: this draft is not current beyond its expiry date for comments. |
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| Price | £20.00 |
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