pnBAS CEN ISO/TS 5798:2025 In vitro diagnostic test systems - Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS CEN/TS 17981-1:2025 In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examination
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS CEN/TS 17981-2:2025 In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN 17854:2025 Antimicrobial wound dressings - Requirements and test method
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN 455-1+A2:2025 Medical gloves for single use - Part 1: Requirements and testing for freedom of holes
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN 455-2:2025 Medical gloves for single use - Part 2: Requirements and testing for physical properties
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN 455-3:2025 Medical gloves for single use - Part 3: Requirements and testing for biological evaluation
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN 556-1:2025 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN ISO 10555-1:2025 Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN ISO 10555-4:2025 Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN ISO 10993-17:2025 Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS 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
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS 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
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS 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
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN ISO 11979-7:2025 Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations of intraocular lenses for the correction of aphakia
pnBAS 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
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS 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
30.20
BAS/TC 25
26.03.2025
07.04.2025
pnBAS EN ISO 18113-1:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements
