ISO 9713:2002
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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Neurosurgical implants Self-closing intracranial aneurysm clips
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12-01-2022
English, French
05-09-2002
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ISO 9713:2002 describes characteristics of self-closing aneurysm clips intended for permanent intracranial implantation and specifies requirements for marking, packaging, sterilization and for labelling and accompanying documentation. In addition it gives a method for the measurement of closing force.
ISO 9713:2002 is not applicable to malleable clips, or clips intended to be used during the course of surgery and removed before wound closure (temporary clips).
| DevelopmentNote |
Supersedes ISO/FDIS 9713 (09/2002)
|
| DocumentType |
Standard
|
| Pages |
7
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| DS EN ISO 9713 : 2009 | Identical |
| DIN EN ISO 9713:2009-08 | Identical |
| NBN EN ISO 9713 : 2009 | Identical |
| NEN ISO 9713 : 2002 | Identical |
| NEN EN ISO 9713 : 2010 | Identical |
| NS EN ISO 9713 : 2009 | Identical |
| I.S. EN ISO 9713:2009 | Identical |
| PN EN ISO 9713 : 2009 | Identical |
| SN EN ISO 9713 : 2009 | Identical |
| UNI EN ISO 9713 : 2009 | Identical |
| IS 14139 : 2008(R2018) | Identical |
| BS EN ISO 9713:2009 | Identical |
| UNE-EN ISO 9713:2009 | Identical |
| EN ISO 9713:2009 | Identical |
| NF EN ISO 9713 : 2009 | Identical |
| UNE-EN ISO 9713:2004 | Identical |
| BS 6788-3:1990 | Similar to |
| BS ISO 16142-1:2016 | Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
| ISO 16142-1:2016 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
| ISO 23552-1:2007 | Safety and control devices for gas and/or oil burners and gas and/or oil appliances — Particular requirements — Part 1: Fuel/air ratio controls, electronic type |
| ISO 5832-6:1997 | Implants for surgery Metallic materials Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy |
| ISO 5832-5:2005 | Implants for surgery Metallic materials Part 5: Wrought cobalt-chromium-tungsten-nickel alloy |
| ISO 5832-3:2016 | Implants for surgery Metallic materials Part 3: Wrought titanium 6-aluminium 4-vanadium alloy |
| ISO 5832-8:1997 | Implants for surgery Metallic materials Part 8: Wrought cobalt-nickel-chromium-molybdenum- tungsten-iron alloy |
| ISO 14630:2012 | Non-active surgical implants — General requirements |
| ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants General requirements |
| ISO 5832-2:1999 | Implants for surgery Metallic materials Part 2: Unalloyed titanium |
| ISO 5832-7:2016 | Implants for surgery — Metallic materials — Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy |
| ISO 15223:2000 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied |
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