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.
Implants for surgery — Materials — Simulated body fluid (SBF) preparation procedure and test method to detect apatite formation in SBF for initial screening of bone-contacting implant materials
40.00 DIS registered
Additive manufacturing for medical — General principles — Additive manufacturing of non-active implants
40.20 DIS ballot initiated: 12 weeks
Implants for surgery — Components for partial and total knee joint prostheses — Part 2: Articulating surfaces made of metal, ceramic and plastics materials
40.60 Close of voting
Prosthetics and orthotics — Limb deficiencies — Part 3: Method of describing the residual limb after upper limb amputation
40.60 Close of voting
Non-active surgical implants — Mammary implants — Specific requirements
50.00 Final text received or FDIS registered for formal approval
Non-active surgical implants — General requirements
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Prosthetics — Testing of ankle-foot devices and foot units — Requirements and test methods
50.00 Final text received or FDIS registered for formal approval
Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
50.00 Final text received or FDIS registered for formal approval
Cardiovascular implants and extracorporeal systems — Cardiac valve repair devices
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Neurosurgical implants — Sterile, single-use hydrocephalus shunts
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Cardiovascular implants and artificial organs — Blood-gas exchangers (oxygenators)
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Sizing parameters of surgical valve prostheses: Requirements regarding the application of ISO 5840-2
60.60 Standard published
Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information
60.60 Standard published
Implants for surgery — Essential principles of safety and performance
60.60 Standard published
Tissue-engineered medical products — Evaluation of anisotropic structure of articular cartilage using DT (Diffusion Tensor)-MR Imaging
60.60 Standard published
Non-active surgical implants — Implant coating — Part 2: Reference standards related to coatings
60.60 Standard published
Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass
60.60 Standard published
Guidance for uncertainty analysis regarding the application of ISO/TS 10974
90.93 Standard confirmed
