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ISO 19001
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
Edition
2013-03
ISO 15223-1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements
Edition
2021-07
ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements
Edition
2022-10
BS EN 15267-2
Air quality. Assessment of air quality monitoring equipment. Initial assessment of the manufacturer's quality management system and post certification surveillance for the manufacturing process
Edition
2023-07-07
BS EN ISO 17664-1
Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices. Critical and semi-critical medical devices
Edition
2021-09-01
BS EN 45502-1
Implants for surgery. Active implantable medical devices. General requirements for safety, marking and for information to be provided by the manufacturer
Edition
2015-06-30
PD CEN/TR 16625
Flexible sheets for waterproofing. Statistical definition of manufacturer's limiting value and declared value (MLV and MDV). 95 % Statistic
Edition
2013-12-31
BS EN 818-6+A1
Short link chain for lifting purposes. Safety. Chain slings. Specification for information for use and maintenance to be provided by the manufacturer
Edition
2000-04-15
BS EN ISO 18113-4
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for self-testing
Edition
2024-06-12
BS EN ISO 18113-5
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling). Part 5: In vitro diagnostic instruments for self-testing
Edition
2024-06-12