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Number of results 880
UNE-EN 455-1:2020+A2:2025
Medical gloves for single use - Part 1: Requirements and testing for freedom of holes
UNE-EN ISO 17665:2025
Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)
UNE-EN 1865-2:2025
Patient handling equipment used in ambulances - Part 2: Power assisted stretcher
UNE-EN ISO 23500-1:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 1: General requirements (ISO 23500-1:2024)
UNE-EN ISO 23500-2:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2024)
UNE-EN 556-1:2025
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
UNE-EN 455-2:2024
Medical gloves for single use - Part 2: Requirements and testing for physical properties
UNE-EN ISO 23500-3:2024
Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2024)
UNE-EN ISO 13408-1:2024
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023)
UNE-EN ISO 23500-4:2024
Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2024)
UNE-EN ISO 23500-5:2024
Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2024)
UNE-EN ISO 8362-2:2024
Injection containers and accessories - Part 2: Closures for injection vials (ISO 8362-2:2024)
UNE-EN ISO 17664-2:2024
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)
UNE-EN ISO 11139:2020/A1:2024
Sterilization of health care products - Vocabulary of terms used in sterilization and related equipment and process standards - Amendment 1: Amended and additional terms and definitions (ISO 11139:2018/Amd 1:2024)
UNE-EN ISO 81060-2:2020/A2:2024
Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type - Amendment 2 (ISO 81060-2:2018/Amd 2:2024)
UNE-EN 17430:2024
Chemical disinfectants and antiseptics - Hygienic handrub virucidal - Test method and requirements (phase 2/step 2)
UNE-EN 17854:2024
Antimicrobial wound dressings - Requirements and test method
UNE-EN ISO 8536-13:2024
Infusion equipment for medical use - Part 13: Graduated flow regulators for single use with fluid contact (ISO 8536-13:2024) (Endorsed by Asociación Española de Normalización in November of 2024.)
UNE-EN ISO 7199:2024
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2024) (Endorsed by Asociación Española de Normalización in October of 2024.)
UNE-EN ISO 15378:2018/A1:2024
Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) - Amendment 1: Climate action changes (ISO 15378:2017/Amd 1:2024)
UNE-EN 1789:2021+A1:2024
Medical vehicles and their equipment - Road ambulances
UNE-EN ISO 10555-4:2024
Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2023)
UNE-EN ISO 10555-1:2024
Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements (ISO 10555-1:2023)
UNE-EN 455-3:2024
Medical gloves for single use - Part 3: Requirements and testing for biological evaluation