Use the form below to find particular standards or projects. Enter your criteria for searching (single or in combination) in the fields below and press the button “Search”. You can also search using the Advance Search facility.
Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes - Amendment 1 (ISO 5840-2:2021/DAM 1:2024)
40.60 Close of voting
Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques (ISO 5840-3:2021)
60.60 Standard published
Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques - Amendment 1 (ISO 5840 3:2021/DAM 1:2024)
40.60 Close of voting
Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components (ISO 7197:2006, including Cor 1:2007)
60.60 Standard published
Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)
60.60 Standard published
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2016)
60.60 Standard published
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) - Amendment 1: Connectors (ISO 7199:2016/Amd 1:2020)
60.60 Standard published
Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
60.60 Standard published
Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2022)
60.60 Standard published
Non-active surgical implants - General requirements (ISO/FDIS 14630:2024)
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants (ISO/FDIS 21535:2023)
60.55 Ratification completed (DOR)
Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO/FDIS 21536:2023)
60.55 Ratification completed (DOR)
Preparation and quality management of fluids for haemodialysis and related therapies - Part 1: General requirements (ISO/FDIS 23500-1:2024)
50.60 Close of voting. Proof returned by secretariat
Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO/FDIS 23500-2:2024)
50.60 Close of voting. Proof returned by secretariat
Neurosurgical implants - Sterile, single-use hydrocephalus shunts (ISO/FDIS 7197:2024)
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Non-active surgical implants - Mammary implants - Particular requirements (ISO/DIS 14607:2023)
45.99 Dispatch of FV draft to CCMC
External limb prostheses and external orthoses - Requirements and test methods (ISO/DIS 22523:2022)
40.60 Close of voting
Prosthetics - Testing of ankle-foot devices and foot units - Requirements and test methods (ISO/DIS 22675:2021)
45.99 Dispatch of FV draft to CCMC