- IEC 60601-2-75, Edition 1.0, Medical electrical equipment - Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment
- IEC 60601-4-1, Edition 1.0, Medical electrical equipment - Part 4-1: Guidance and interpretation - Medical electrical equipment and medical electrical systems employing a degree of autonomy
- ISO 80002-2, 1st Edition, Medical device software - Part 2: Validation of software for medical device quality systems
- PD IEC 60601-4-1, 2017 Edition, Medical electrical equipment. Guidance and interpretation. Medical electrical equipment and medical electrical systems employing a degree of autonomy
- UNE EN ISO 15223-1, 2017 Edition, Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
- DIN EN ISO 5366-1, Withdrawn and replace by DIN EN ISO 5366, Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults
- ISO 80601-2-74, 1st Edition, Medical electrical equipment - Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
- BS EN 80369-5, 2016 Edition, Small-bore connectors for liquids and gases in healthcare applications. Connectors for limb cuff inflation applications
- ISO 7886-1, 2nd Edition, Sterile hypodermic syringes for single use - Part 1: Syringes for manual use
- UNE EN ISO 7153-1, 2017 Edition, Surgical instruments - Materials - Part 1: Metals
- IEC 60601-2-2, Edition 6.0, Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories
- IEC 60601-2-2-RL, Edition 6.0, Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories
- UNE EN ISO 7153-1, 2017 Edition, Surgical instruments - Materials - Part 1: Metals
- ANSI/AAMI/ISO-7198, 2016 Edition, Cardiovascular implants - Tubular vascular prostheses
- ANSI/AAMI/ISO-7199, 2016 Edition, Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
- ASTM F1828, 2017 Edition, Standard Specification for Ureteral Stents
- ASTM F2064, 2017 Edition, Standard Guide for Characterization and Testing of Alginates as Starting Materials Intended for Use in Biomedical and Tissue Engineered Medical Product Applications
- ASTM F2180, 2017 Edition, Standard Specification for Metallic Implantable Strands and Cables
- ASTM F2706, 20107 Edition, Standard Test Methods for Occipital-Cervical and Occipital-Cervical-Thoracic Spinal Implant Constructs in a Vertebrectomy Model
- ASTM F2902, 2016 Edition with Editorial Correction (E1), Standard Guide for Assessment of Absorbable Polymeric Implants
- ASTM F384, 2017 Edition, Standard Specifications and Test Methods for Metallic Angled Orthopedic Fracture Fixation Devices
- ASTM F543, 2017 Edition, Standard Specification and Test Methods for Metallic Medical Bone Screws
- ASTM F67, 2013 Edition Reapproved in 2017, Standard Specification for Unalloyed Titanium, for Surgical Implant Applications (UNS R50250, UNS R50400, UNS R50550, UNS R50700)
- BS ISO 18192-3, 2017 Edition, Implants for surgery. Wear of total intervertebral spinal disc prostheses. Impingement-wear testing and corresponding environmental conditions for test of lumbar prostheses under adverse kinematic conditions
- BS ISO 19233-1, 2017 Edition, Implants for surgery. Orthopaedic joint prosthesis. Procedure for producing parametric 3D bone models from CT data of the knee
- ISO 18192-3, 1st Edition, Implants for surgery - Wear of total intervertebral spinal disc prostheses - Part 3: Impingement-wear testing and corresponding environmental conditions for test of lumbar prostheses under adverse kinematic conditions
- ISO 14708-3, 1st Edition, Implants for surgery - Orthopaedic joint prosthesis - Part 1: Procedure for producing parametric 3D bone models from CT data of the knee
- ISO 11491, 1st Edition, Implants for surgery - Determination of impact resistance of ceramic femoral heads for hip joint prostheses
- ISO 19233-1, 1st Edition, Implants for surgery - Orthopaedic joint prosthesis - Part 1: Procedure for producing parametric 3D bone models from CT data of the knee
- IEC 60601-2-43-AM1, Edition 2.0 with Amendment 1, Amendment 1 - Medical electrical equipment - Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures
- IEC 60601-2-65-AM1, Edition 1.0 with Amendment 1, Amendment 1 - Medical electrical equipment - Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral X-ray equipment
- IEC 60601-2-28, Edition 3.0, Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis
- IEC 60601-2-28-RL, Edition 1.0, Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis
- ISO 19614, 1st Edition, Traditional Chinese medicine - Pulse graph force transducer
- BS EN ISO 11979-8, 2017 Edition, Ophthalmic implants. Intraocular lenses. Fundamental requirements
- EN ISO 11979-8, 2017 Edition - See BS or DIN Edition, Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements
- ISO 10939, 3rd Edition, Ophthalmic instruments - Slit-lamp microscopes
- ISO 11979-8, 3rd Edition, Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements
- ISO 15798, 3rd Edition, Ophthalmic implants - Ophthalmic viscosurgical devices
- ISO 15798-AM1, 3rd Edition with Amendment 1, AMENDMENT 1, Ophthalmic implants - Ophthalmic viscosurgical devices
- ISO 18476, 1st Edition, Ophthalmic optics and instruments - Free form technology - Spectacle lenses and measurement
- ISO 22979, 2nd Edition, Ophthalmic implants - Intraocular lenses - Guidance on assessment of the need for clinical investigation of intraocular lens design modifications
- BS ISO 19611, 2017 Edition, Traditional Chinese medicine. Air extraction cupping device
- DIN EN ISO 19054, 2017 Edition, Rail systems for supporting medical equipment
- ISO 19611, 1st Edition, Traditional Chinese medicine - Air extraction cupping device
- ISO 20308, 1st Edition, Traditional Chinese medicine - Gua Sha instruments
- ISO 20498-2, 1st Edition, Traditional Chinese medicine - Computerized tongue image analysis system - Part 2: Light environment
For more standards like these, please refer to our Document Center List of Standards on Medical Equipment.
