Showing 41-60 of 78 items.
Standard referenceStage codeBAS/TCReal dateForseen date for next stage code
  
psBAS CEN/TS 17981-2:2025
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN 17854:2025
Antimicrobial wound dressings - Requirements and test method		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN 455-1+A2:2025
Medical gloves for single use - Part 1: Requirements and testing for freedom of holes		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN 455-2:2025
Medical gloves for single use - Part 2: Requirements and testing for physical properties		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN 455-3:2025
Medical gloves for single use - Part 3: Requirements and testing for biological evaluation		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN 556-1:2025
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 10555-1:2025
Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 10555-4:2025
Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 10993-17:2025
Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 11139/A1:2025
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 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 11607-1/A1:2025
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems - Amendment 1: Application of risk management 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 11607-2/A1:2025
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1: Application of risk management 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 11979-7:2025
Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations of intraocular lenses for the correction of aphakia 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 13408-1:2025
Aseptic processing of health care products - Part 1: General requirements 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 15002:2025
Flow control devices for connection to a medical gas supply system 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 17664-2:2025
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 		50.99BAS/TC 2513.06.202513.06.2025
psBAS 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 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 18113-1:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 18113-2:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use 		50.99BAS/TC 2513.06.202513.06.2025
psBAS EN ISO 18113-3:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use 		50.99BAS/TC 2513.06.202513.06.2025