BS EN ISO 10993-6:2016
Current
The latest, up-to-date edition.
Biological evaluation of medical devices Tests for local effects after implantation
Hardcopy , PDF
English
31-12-2016
Committee |
CH/194
|
DevelopmentNote |
Supersedes BS EN 30993-6. (05/2007) Supersedes 14/30261590 DC. (12/2016)
|
DocumentType |
Standard
|
Pages |
46
|
PublisherName |
British Standards Institution
|
Status |
Current
|
Supersedes |
This part of ISO10993 specifies test methods for the assessment of the local effects after implantation of biomaterials intended for use in medical devices.
This part of ISO10993 applies to materials that are
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solid and non-absorbable,
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non-solid, such as porous materials, liquids, gels, pastes, and particulates, and
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degradable and/or absorbable, which may be solid or non-solid.
The test sample is implanted into a site and animal species appropriate for the evaluation of the biological safety of the material. These implantation tests are not intended to evaluate or determine the performance of the test sample in terms of mechanical or functional loading. This part of ISO10993 can also be applied to medical devices that are intended to be used topically in clinical indications where the surface or lining might have been breached, in order to evaluate local tissue responses.
The local effects are evaluated by a comparison of the tissue response caused by a test sample to that caused by control materials used in medical devices whose clinical acceptability and biocompatibility characteristics have been established. The objective of the test methods is to characterize the history and evolution of the tissue response after implantation of a medical device/biomaterial including final integration or absorption/degradation of the material. In particular for degradable/absorbable materials, the degradation characteristics of the material and the resulting tissue response should be determined.
This part of ISO10993 does not deal with systemic toxicity, carcinogenicity, teratogenicity or mutagenicity. However, the long-term implantation studies intended for evaluation of local biological effects might provide insight into some of these properties. Systemic toxicity studies conducted by implantation might satisfy the requirements of this part of ISO10993. When conducting combined studies for evaluating local effects and systemic effects, the requirements of both standards is to be fulfilled.
Standards | Relationship |
NS EN ISO 10993-6 : 2016 | Identical |
NEN EN ISO 10993-6 : 2016 | Identical |
NF EN ISO 10993-6 : 2017 | Identical |
EN ISO 10993-6:2016 | Identical |
NBN EN ISO 10993-6 : 2009 | Identical |
ISO 10993-6:2016 | Identical |
DIN EN ISO 10993-6:2009-08 | Identical |
SN EN ISO 10993-6 : 2017 | Identical |
UNE-EN ISO 10993-6:2017 | Identical |
UNI EN ISO 10993-6 : 2009 | Identical |
I.S. EN ISO 10993-6:2016 | Identical |
DIN EN ISO 10993-6:2017-09 | Identical |
BS PAS 84(2008) : 2008 | REGENERATIVE MEDICINE - GLOSSARY |
ISO 5832-1:2016 | Implants for surgery — Metallic materials — Part 1: Wrought stainless steel |
ISO 10993-4:2017 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
ISO 10993-16:2017 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables |
ASTM F 1983 : 2014 : REDLINE | Standard Practice for Assessment of Selected Tissue Effects of Absorbable Biomaterials for Implant Applications |
EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
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 10993-2:2006 | Biological evaluation of medical devices — Part 2: Animal welfare requirements |
ISO 7405:2008 | Dentistry Evaluation of biocompatibility of medical devices used in dentistry |
EN ISO 10993-4:2017 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) |
ISO 5832-8:1997 | Implants for surgery Metallic materials Part 8: Wrought cobalt-nickel-chromium-molybdenum- tungsten-iron alloy |
ISO 5832-4:2014 | Implants for surgery — Metallic materials — Part 4: Cobalt-chromium-molybdenum casting alloy |
ISO 6474-1:2010 | Implants for surgery Ceramic materials Part 1: Ceramic materials based on high purity alumina |
ISO 10993-11:2017 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
ISO 10993-12:2012 | Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
ISO 5834-2:2011 | Implants for surgery Ultra-high-molecular-weight polyethylene Part 2: Moulded forms |
ASTM F 748 : 2016 : REDLINE | Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
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 10993-9:2009 | Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
ISO 11979-5:2006 | Ophthalmic implants Intraocular lenses Part 5: Biocompatibility |
ISO 6474-2:2012 | Implants for surgery Ceramic materials Part 2: Composite materials based on a high-purity alumina matrix with zirconia reinforcement |
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