NBR 15723-4 : 2010
Withdrawn
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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IMPLANTS FOR SURGERY - POLYMERIC MATERIALS - PART 4: SPECIFICATION FOR POROUS POLYETHYLENE POLYMERS
Published date
12-01-2013
Publisher
Withdrawn date
15-12-2020
Superseded by
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| Committee |
CB-26
|
| DocumentType |
Standard
|
| PublisherName |
Brazilian Standards
|
| Status |
Withdrawn
|
| SupersededBy |
| ISO 10993-3:2014 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity |
| 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 |
| ISO/TS 10993-20:2006 | Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devices |
| ISO 1628-1:2009 | Plastics — Determination of the viscosity of polymers in dilute solution using capillary viscometers — Part 1: General principles |
| ISO 10993-13:2010 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices |
| ASTM D 1238 : 2013 : REDLINE | Standard Test Method for Melt Flow Rates of Thermoplastics by Extrusion Plastometer |
| ASTM D 792 : 2013 : REDLINE | Standard Test Methods for Density and Specific Gravity (Relative Density) of Plastics by Displacement |
| ISO 10993-2:2006 | Biological evaluation of medical devices — Part 2: Animal welfare requirements |
| ISO 527-2:2012 | Plastics — Determination of tensile properties — Part 2: Test conditions for moulding and extrusion plastics |
| ASTM D 256 : 2015-10 | TEST METHODS FOR DETERMINING THE IZOD PENDULUM IMPACT RESISTANCE OF PLASTICS |
| ISO 10993-18:2005 | Biological evaluation of medical devices — Part 18: Chemical characterization of materials |
| ISO/TS 10993-19:2006 | Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials |
| ASTM D 696 : 2016 : REDLINE | Standard Test Method for Coefficient of Linear Thermal Expansion of Plastics Between −30°C and 30°C with a Vitreous Silica Dilatometer |
| ISO 180:2000 | Plastics — Determination of Izod impact strength |
| ISO 10993-10:2010 | Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization |
| 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 10993-7:2008 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals |
| ASTM D 790 : 2017 : REDLINE | Standard Test Methods for Flexural Properties of Unreinforced and Reinforced Plastics and Electrical Insulating Materials |
| ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances |
| ISO 1183-1:2012 | Plastics — Methods for determining the density of non-cellular plastics — Part 1: Immersion method, liquid pyknometer method and titration method |
| ASTM F 748 : 2016 : REDLINE | Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices |
| ISO 1183-2:2004 | Plastics — Methods for determining the density of non-cellular plastics — Part 2: Density gradient column method |
| ISO 1183-3:1999 | Plastics — Methods for determining the density of non-cellular plastics — Part 3: Gas pyknometer method |
| ISO 10993-1:2009 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process |
| ASTM D 648 : 2016 | Standard Test Method for Deflection Temperature of Plastics Under Flexural Load in the Edgewise Position |
| ISO 10993-9:2009 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products |
| ASTM D 695 : 2015 : REDLINE | Standard Test Method for Compressive Properties of Rigid Plastics |
| ASTM D 570 : 1998 : R2018 | Standard Test Method for Water Absorption of Plastics |
| ISO 527-3:1995 | Plastics — Determination of tensile properties — Part 3: Test conditions for films and sheets |
| ISO 178:2010 | Plastics — Determination of flexural properties |
| ISO 1133:2005 | Plastics — Determination of the melt mass-flow rate (MFR) and the melt volume-flow rate (MVR) of thermoplastics |
| ASTM D 638 : 2014 : REDLINE | Standard Test Method for Tensile Properties of Plastics |
| ISO 10993-6:2016 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation |
| ISO 527-1:2012 | Plastics — Determination of tensile properties — Part 1: General principles |
| ASTM D 4000 : 2016 : REDLINE | Standard Classification System for Specifying Plastic Materials |
Summarise
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