NBR 15723-4 : 2010
Withdrawn
Withdrawn
View Superseded by
IMPLANTS FOR SURGERY - POLYMERIC MATERIALS - PART 4: SPECIFICATION FOR POROUS POLYETHYLENE POLYMERS
Published date
01-12-2013
Publisher
Withdrawn date
12-15-2020
Superseded by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Withdrawn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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