- ASTM F1634, 1995 Edition Reapproved in 2016, Standard Practice for In-Vitro Environmental Conditioning of Polymer Matrix Composite Materials and Implant Devices
- ASTM F2777, 2016 Edition, Standard Test Method for Evaluating Knee Bearing (Tibial Insert) Endurance and Deformation Under High Flexion
- BS EN ISO 10328, 2016 Edition, Prosthetics. Structural testing of lower-limb prostheses. Requirements and test methods
- BS EN ISO 22675, 2016 Edition, Prosthetics. Testing of ankle-foot devices and foot units. Requirements and test methods
- BS ISO 5832-1, 2016 Edition, Implants for surgery. Metallic materials. Wrought stainless steel
- BS ISO 7206-12, 2016 Edition, Implants for surgery. Partial and total hip joint prostheses. Deformation test method for acetabular shells
- BS ISO 7206-13, 2016 Edition, Implants for surgery. Partial and total hip joint prostheses. Determination of resistance to torque of head fixation of stemmed femoral components
- BS ISO 7207-2, 2011 Edition with Amendment 1, Implants for surgery. Components for partial and total knee joint prostheses. Articulating surfaces made of metal, ceramic and plastics materials
- BS ISO 14242-2, 2016 Edition, Implants for surgery. Wear of total hip-joint prostheses. Methods of measurement
- BS ISO 14243-2, 2016 Edition, Implants for surgery. Wear of total knee-joint prostheses. Methods of measurement
- BS ISO 15674, 2016 Edition, Cardiovascular implants and artificial organs. Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
- BS ISO 15675, 2016 Edition, Cardiovascular implants and artificial organs. Cardiopulmonary bypass systems. Arterial blood line filters
- BS ISO 15676, 2016 Edition, Cardiovascular implants and artificial organs. Requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO)
- BS ISO 18241, 2016 Edition, Cardiovascular implants and extracorporeal systems. Cardiopulmonary bypass systems. Venous bubble traps
- BS ISO 18242, 2016 Edition, Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
- ISO 5832-1, 5th Edition, Implants for surgery - Metallic materials - Part 1: Wrought stainless steel
- ISO 7198, 2nd Edition, Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
- ISO 7206-2, Amendment 1 for the 3rd Edition, Implants for Surgery - Partial and Total Hip Joint Prostheses - Part 2: Articulating Surfaces Made of Metallic, Ceramic and Plastics Materials
- ISO 7206-12, 1st Edition, Implants for surgery - Partial and total hip joint prostheses - Part 12: Deformation test method for acetabular shells
- ISO 7206-13, 1st Edition, Implants for surgery - Partial and total hip joint prostheses - Part 13: Determination of resistance to torque of head fixation of stemmed femoral components
- ISO 7207-2, Amendment 1 for the 2nd Edition, Implants for surgery - Components for partial and total knee joint prostheses - Part 2: Articulating surfaces made of metal, ceramic and plastics materials
- ISO 14242-2, 2nd Edition, Implants for surgery - Wear of total hip-joint prostheses - Part 2: Methods of measurement
- ISO 14243-2, 3rd Edition, Implants for surgery - Wear of total knee-joint prostheses - Part 2: Methods of measurement
- ISO 15674, 3rd Edition, Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
- ISO 15675, 3rd Edition, Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filters
- ISO 15676, 2nd Edition, Cardiovascular implants and artificial organs - Requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO)
- ISO 18241, 1st Edition, Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble traps
- ISO 18242, 1st Edition, Cardiovascular implants and extracorporeal systems - Centrifugal blood pumps
- ISO 19024, 1st Edition, Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass
For more standards like these, please refer to our Document Center List of Standards on Implants for Surgery, Prosthetics, and Orthotics.
