ASTM F 2065 : 2000 : R2006
|
Standard Practice for Testing for Alternative Pathway Complement Activation in Serum by Solid Materials |
ASTM F 2068 : 2015 : REDLINE
|
Standard Specification for Femoral Prostheses—Metallic Implants |
ASTM F 1088 : 2004 : REV A
|
Standard Specification for Beta-Tricalcium Phosphate for Surgical Implantation |
ASTM F 2665 : 2009
|
Standard Specification for Total Ankle Replacement Prosthesis |
ASTM F 1581:2008
|
Standard Specification for Composition of Anorganic Bone for Surgical Implants |
ASTM F 1781 : 2015 : REDLINE
|
Standard Specification for Elastomeric Flexible Hinge Finger Total Joint Implants |
ASTM F 813 : 2007
|
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices |
ASTM F 1828 : 2017 : REDLINE
|
Standard Specification for Ureteral Stents |
ASTM F 1185 : 2003
|
Standard Specification for Composition of Hydroxylapatite for Surgical Implants |
ASTM F 2848 : 2017 : REDLINE
|
Standard Specification for Medical-Grade Ultra-High Molecular Weight Polyethylene Yarns |
ASTM F 623 : 1999 : R2006
|
Standard Performance Specification for Foley Catheter |
ASTM F 602 : 2009
|
Standard Criteria for Implantable Thermoset Epoxy Plastics |
ASTM F 1185 : 2003 : R2014
|
Standard Specification for Composition of Hydroxylapatite for Surgical Implants |
ASTM F 2065 : 2000 : R2010
|
Standard Practice for Testing for Alternative Pathway Complement Activation in Serum by Solid Materials (Withdrawn 2016) |
ASTM F 641 : 2009 : R2014
|
Standard Specification for Implantable Epoxy Electronic Encapsulants |
ASTM F 665 : 2009 : R2015
|
Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application |
ASTM F 1027 : 1986 : R2017
|
Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices (Withdrawn 2023) |
ASTM F 1904 : 2014 : REDLINE
|
Standard Practice for Testing the Biological Responses to Particles in vivo |
ASTM F 3089 : 2014
|
Standard Guide for Characterization and Standardization of Polymerizable Collagen-Based Products and Associated Collagen-Cell Interactions |
ASTM F 1357 : 2014 : REDLINE
|
Standard Specification for Articulating Total Wrist Implants |
ASTM F 1713 : 2008 : R2013
|
Standard Specification for Wrought Titanium-13Niobium-13Zirconium Alloy for Surgical Implant Applications (UNS R58130) |
ASTM F 2665 : 2009 : R2014
|
Standard Specification for Total Ankle Replacement Prosthesis |
ASTM E 2524 : 2008
|
Standard Test Method for Analysis of Hemolytic Properties of Nanoparticles |
ASTM F 1088 : 2004 : REV A : R2010
|
Standard Specification for Beta-Tricalcium Phosphate for Surgical Implantation |
ASTM F 2900 : 2011
|
Standard Guide for Characterization of Hydrogels used in Regenerative Medicine (Withdrawn 2020) |
ASTM F 1925 : 2017 : REDLINE
|
Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants |
ASTM F 1906 : 1998 : R2003
|
Standard Practice for Evaluation of Immune Responses In Biocompatibility Testing Using ELISA Tests, Lymphocyte, Proliferation, and Cell Migration (Withdrawn 2011) |
ASTM F 1088:2004
|
Standard Specification for Beta-Tricalcium Phosphate for Surgical Implantation |
ASTM F 1542 : 1994 : R2000
|
Standard Specification for the Requirements and Disclosure of Self-Closing Aneurysm Clips (Withdrawn 2009) |
ASTM F 1538 : 2003 : R2009
|
Standard Specification for Glass and Glass Ceramic Biomaterials for Implantation |
ASTM F 624 : 2009 : R2015 : EDT 1
|
Standard Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Biomedical Applications |
ASTM F 1185 : 2003 : R2009
|
Standard Specification for Composition of Hydroxylapatite for Surgical Implants |
ASTM F 1581 : 2008 : R2012
|
Standard Specification for Composition of Anorganic Bone for Surgical Implants |
ASTM F 1027 : 1986 : R2007
|
Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices |
ASTM F 2384 : 2010
|
Standard Specification for Wrought Zirconium-2.5Niobium Alloy for Surgical Implant Applications (UNS R60901) |
ASTM F 2042 : 2000 : R2005
|
Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part II - Crosslinking and Fabrication |
ASTM F 2581 : 2012
|
Standard Specification for Wrought Nitrogen Strengthened 11Manganese-17Chromium-3Molybdenum Low-Nickel Stainless Steel Alloy Bar and Wire for Surgical Implants (UNS S29225) |
ASTM F 1672 : 2014 : REDLINE
|
Standard Specification for Resurfacing Patellar Prosthesis |
ASTM F 2347 : 2015 : REDLINE
|
Standard Guide for Characterization and Testing of Hyaluronan as Starting Materials Intended for Use in Biomedical and Tissue Engineered Medical Product Applications |
ASTM F 2042 : 2000 : EDT 1
|
Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part II - Crosslinking and Fabrication |
ASTM F 895 : 2011 : R2016
|
Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity |
ASTM E 2524 : 2008 : R2013
|
Standard Test Method for Analysis of Hemolytic Properties of Nanoparticles (Withdrawn 2022) |
ASTM F 2064 : 2017 : REDLINE
|
Standard Guide for Characterization and Testing of Alginates as Starting Materials Intended for Use in Biomedical and Tissue Engineered Medical Product Applications |
ASTM F 2581 : 2012 : R2017
|
Standard Specification for Wrought Nitrogen Strengthened 11Manganese-17Chromium-3Molybdenum Low-Nickel Stainless Steel Alloy Bar and Wire for Surgical Implants (UNS S29225) |
ASTM F 2567 : 2006 : R2010
|
Standard Practice for Testing for Classical Pathway Complement Activation in Serum by Solid Materials (Withdrawn 2016) |
ASTM F 755 : 1999 : EDT 1
|
Standard Specification for Selection of Porous Polyethylene for Use in Surgical Implants |
ASTM F 881 : 1994 : R2000
|
Standard Specification for Silicone Elastomer Facial Implants |
ASTM F 2565 : 2013 : REDLINE
|
Standard Guide for Extensively Irradiation-Crosslinked Ultra-High Molecular Weight Polyethylene Fabricated Forms for Surgical Implant Applications |
ASTM F 2887 : 2017 : REDLINE
|
Standard Specification for Total Elbow Prostheses |
ASTM F 2150 : 2013 : REDLINE
|
Standard Guide for Characterization and Testing of Biomaterial Scaffolds Used in Tissue-Engineered Medical Products |
ASTM F 750 : 1987 : R1996
|
Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse |
ASTM F 813 : 2007 : R2012
|
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices |
ASTM F 1439 : 2003
|
Standard Guide for Performance of Lifetime Bioassay for the Tumorigenic Potential of Implant Materials |
ASTM F 982 : 1986 : R2002
|
Standard Specification for Disclosure of Characteristics of Surgically Implanted Clamps for Carotid Occlusion |
ASTM F 623 : 1999 : R2013
|
Standard Performance Specification for Foley Catheter |
ASTM F 763 : 2004
|
Standard Practice for Short-Term Screening of Implant Materials |
ASTM F 2026 : 2017 : REDLINE
|
Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications |
ASTM F 988 : 1986
|
Guide for Specifying Carbon-Fiber Randomly Reinforced Ultra-High-Molecular-Weight Polyethylene for Medical Devices (Withdrawn 1992) |
ASTM F 641 : 2009
|
Standard Specification for Implantable Epoxy Electronic Encapsulants |
ASTM F 2759 : 2011 : REDLINE
|
Standard Guide for Assessment of the Ultra High Molecular Weight Polyethylene (UHMWPE) Used in Orthopedic and Spinal Devices |
ASTM F 1581 : 2008 : R2016
|
Standard Specification for Composition of Anorganic Bone for Surgical Implants |
ASTM F 1873 : 1998
|
Standard Specification for High-Purity Dense Yttria Tetragonal Zirconium Oxide Polycrystal (Y-TZP) for Surgical Implant Applications (Withdrawn 2007) |
ASTM F 2051 : 2000 : R2014
|
Standard Specification for Implantable Saline Filled Breast Prosthesis |
BS EN ISO 10993-6:2016
|
Biological evaluation of medical devices Tests for local effects after implantation |
I.S. EN ISO 10993-6:2016
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
ASTM F 1538 : 2003
|
Standard Specification for Glass and Glass Ceramic Biomaterials for Implantation |
ASTM F 2097 : 2016 : REDLINE
|
Standard Guide for Design and Evaluation of Primary Flexible Packaging for Medical Products |
ASTM F 639 : 2009 : R2015
|
Standard Specification for Polyethylene Plastics for Medical Applications |
ASTM F 623 : 1999 : EDT 1
|
Standard Performance Specification for Foley Catheter |
ASTM F 1579 : 2002
|
Standard Specification for Polyaryletherketone (PAEK) Polymers for Surgical Implant Applications |
ASTM F 895 : 2011
|
Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity |
ASTM F 1027 : 1986 : R2002
|
Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices |
ASTM F 1713 : 2008
|
Standard Specification for Wrought Titanium-13Niobium-13Zirconium Alloy for Surgical Implant Applications (UNS R58130) |
ANSI/AAMI/ISO 10993-6:2016
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION |
ASTM F 2808 : 2017 : REDLINE
|
Standard Test Method for Performing Behind-the-Knee (BTK) Test for Evaluating Skin Irritation Response to Products and Materials That Come Into Repeated or Extended Contact with Skin |
ASTM F 1855 : 2000
|
Standard Specification for Polyoxymethylene (Acetal) for Medical Applications |
ASTM F 602 : 2009 : R2014
|
Standard Criteria for Implantable Thermoset Epoxy Plastics |
ASTM F 1903 : 2010-07
|
PRACTICE FOR TESTING FOR BIOLOGICAL RESPONSES TO PARTICLES IN VITRO |
ASTM F 1439 : 2003 : R2008
|
Standard Guide for Performance of Lifetime Bioassay for the Tumorigenic Potential of Implant Materials |
ASTM F 750 : 1987 : R2002 : EDT 1
|
Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse |
ASTM F 1088 : 2004 : REV A : EDT 1
|
Standard Specification for Beta-Tricalcium Phosphate for Surgical Implantation |
ASTM F 1813 : 2013 : REDLINE
|
Standard Specification for Wrought Titanium–12 Molybdenum–6 Zirconium–2 Iron Alloy for Surgical Implant (UNS R58120) |
ASTM F 2212 : 2011 : REDLINE
|
Standard Guide for Characterization of Type I Collagen as Starting Material for Surgical Implants and Substrates for Tissue Engineered Medical Products (TEMPs) |
ASTM F 1905 : 1998
|
Standard Practice for Selecting Tests for Determining the Propensity of Materials to Cause Immunotoxicity |
ASTM F 623 : 1999
|
Standard Performance Specification for Foley Catheter |
ASTM F 881 : 1994 : R2006
|
Standard Specification for Silicone Elastomer Facial Implants |
ASTM F 451 : 2016
|
Standard Specification for Acrylic Bone Cement |
ASTM F 755:1999
|
Standard Specification for Selection of Porous Polyethylene for Use in Surgical Implants |
ASTM F 1984 : 1999 : R2003
|
Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials |
ASTM F 2042 : 2000 : R2011
|
Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part II—Crosslinking and Fabrication |
ASTM F 2883 : 2011
|
Standard Guide for Characterization of Ceramic and Mineral Based Scaffolds used for Tissue-Engineered Medical Products (TEMPs) and as Device for Surgical Implant Applications (Withdrawn 2020) |
ASTM F 1905 : 1998 : R2003
|
Standard Practice for Selecting Tests for Determining the Propensity of Materials to Cause Immunotoxicity (Withdrawn 2011) |
ASTM F 750 : 1987 : R2007 : EDT 1
|
Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse |
ASTM F 1439 : 2003 : R2013
|
Standard Guide for Performance of Lifetime Bioassay for the Tumorigenic Potential of Implant Materials |
ASTM F 2567 : 2006
|
Standard Practice for Testing for Classical Pathway Complement Activation in Serum by Solid Materials |
ASTM F 624 : 2009
|
Standard Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Biomedical Applications |
14/30261590 DC : 0
|
BS EN ISO 10993-6 - BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION |
ASTM F 982 : 1986 : R1998
|
Standard Specification for Disclosure of Characteristics of Surgically Implanted Clamps for Carotid Occlusion |
ASTM F 2384 : 2010 : R2016
|
Standard Specification for Wrought Zirconium-2.5Niobium Alloy for Surgical Implant Applications (UNS R60901) |
ASTM F 763 : 2004 : R2010
|
Standard Practice for Short-Term Screening of Implant Materials |
ASTM F 2820 : 2012
|
Standard Specification for Polyetherketoneketone (PEKK) Polymers for Surgical Implant Applications |
ASTM F 1635 : 2016 : REDLINE
|
Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants |
ASTM F 755 : 1999 : R2005
|
Standard Specification for Selection of Porous Polyethylene for Use in Surgical Implants |
ASTM F 2229 : 2012 : REDLINE
|
Standard Specification for Wrought, Nitrogen Strengthened 23Manganese-21Chromium-1Molybdenum Low-Nickel Stainless Steel Alloy Bar and Wire for Surgical Implants (UNS S29108) |
ASTM F 1906 : 1998
|
Standard Practice for Evaluation of Immune Responses In Biocompatibility Testing Using ELISA Tests, Lymphocyte, Proliferation, and Cell Migration |
ASTM F 1027 : 1986 : R1995 : EDT 1
|
Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices |
CSA ISO 10993-6 : 1997(R2009)
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION |
CSA Z323.3.1 : 1982
|
ELECTRICAL AIDS FOR PHYSICALLY DISABLED PERSONS |
ASTM F 665 : 2009
|
Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application |
ASTM F 602 : 2009 : R2015
|
Standard Criteria for Implantable Thermoset Epoxy Plastics |
ASTM F 881 : 1994 : R2014
|
Standard Specification for Silicone Elastomer Facial Implants |
ASTM F 648 : 2014 : REDLINE
|
Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants |
ASTM F 763 : 2004 : R2016
|
Standard Practice for Short-Term Screening of Implant Materials |
ASTM F 2151 : 2001
|
Standard Practice for Assessment of White Blood Cell Morphology After Contact with Materials (Withdrawn 2007) |
ASTM F 1984 : 1999 : R2013
|
Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials |
ASTM F 1579 : 2002 : EDT 1
|
Standard Specification for Polyaryletherketone (PAEK) Polymers for Surgical Implant Applications (Withdrawn 2011) |
ASTM F 2695 : 2012 : REDLINE
|
Standard Specification for Ultra-High Molecular Weight Polyethylene Powder Blended With Alpha-Tocopherol (Vitamin E) and Fabricated Forms for Surgical Implant Applications |
ASTM F 2739 : 2016
|
Standard Guide for Quantifying Cell Viability within Biomaterial Scaffolds |
ASTM F 2051 : 2000
|
Standard Specification for Implantable Saline Filled Breast Prosthesis |
ASTM F 1855 : 2000 : R2005
|
Standard Specification for Polyoxymethylene (Acetal) for Medical Applications |
ASTM F 2042 : 2000
|
Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part II - Crosslinking and Fabrication |
BS EN 30993-6:1995
|
Biological evaluation of medical devices Tests for local effects after implantation |
EN ISO 10993-6:2016
|
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016) |
ASTM F 750 : 1987 : R2012
|
Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse |
ASTM F 749 : 2013 : REDLINE
|
Standard Practice for Evaluating Material Extracts by Intracutaneous Injection in the Rabbit |
ASTM F 1441 : 2003
|
Standard Specification for Soft-Tissue Expander Devices |
ASTM F 1984 : 1999 : R2008
|
Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials |
ASTM F 750 : 1987 : R2007
|
Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse |
ASTM F 604 : 1994
|
Specification for Silicone Elastomers Used in Medical Applications (Withdrawn 2001) |
ASTM F 1027 : 1986 : R2012
|
Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices |
ASTM F 3087 : 2015
|
Standard Specification for Acrylic Molding Resins for Medical Implant Applications |
ASTM F 750 : 1987 : R2002
|
Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse |
ASTM F 2065 : 2000 : EDT 1
|
Standard Practice for Testing for Alternative Pathway Complement Activation in Serum by Solid Materials |
ASTM F 1855 : 2000 : R2011
|
Standard Specification for Polyoxymethylene (Acetal) for Medical Applications |
ASTM F 2091 : 2015 : REDLINE
|
Standard Specification for Acetabular Prostheses |
ASTM F 1441 : 2003 : R2009
|
Standard Specification for Soft-Tissue Expander Devices |
ASTM F 1538 : 2003 : R2017
|
Standard Specification for Glass and Glass Ceramic Biomaterials for Implantation |
ASTM F 2066 : 2018 : REDLINE
|
Standard Specification for Wrought Titanium-15 Molybdenum Alloy for Surgical Implant Applications (UNS R58150) |
ASTM F 703 : 2018
|
Standard Specification for Implantable Breast Prostheses |
ASTM F 982 : 1986 : R2008
|
Standard Specification for Disclosure of Characteristics of Surgically Implanted Clamps for Carotid Occlusion (Withdrawn 2017) |
ASTM F 756 : 2017 : REDLINE
|
Standard Practice for Assessment of Hemolytic Properties of Materials |
ASTM F 1581 : 2008 : EDT 1
|
Standard Specification for Composition of Anorganic Bone for Surgical Implants |
ASTM F 755 : 1999 : R2011
|
Standard Specification for Selection of Porous Polyethylene for Use in Surgical Implants |
ASTM F 1538 : 2003 : EDT 1
|
Standard Specification for Glass and Glass Ceramic Biomaterials for Implantation |
ASTM F 2051 : 2000 : R2006
|
Standard Specification for Implantable Saline Filled Breast Prosthesis |
ASTM F 619 : 2014 : REDLINE
|
Standard Practice for Extraction of Medical Plastics |
ASTM F 1441 : 2003 : R2014
|
Standard Specification for Soft-Tissue Expander Devices |
ASTM F 639 : 2009
|
Standard Specification for Polyethylene Plastics for Medical Applications |
ASTM F 2083 : 2012 : REDLINE
|
Standard Specification for Knee Replacement Prosthesis |
ASTM F 2847 : 2017 : REDLINE
|
Standard Practice for Reporting and Assessment of Residues on Single-Use Implants and Single-Use Sterile Instruments |
DIN EN ISO 10993-6:2009-08
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
ISO 10993-6:2016
|
Biological evaluation of medical devices Part 6: Tests for local effects after implantation |
DIN EN ISO 10993-6:2017-09
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |