In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
Edition 2013-12-15

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)
Edition 2022-01-01

Sectional Specification: Capability approval of manufacturers of printed board assemblies of assessed quality
Edition 1998-01-14

Petroleum, petrochemical and natural gas industries. Scheme for conformity assessment of manufacturers of special materials
Edition 2018-12-04

Thermal spraying - Quality requirements for manufacturers of thermal sprayed coatings
Edition 2021-10-06

Medical devices - Post-market surveillance for manufacturers
Edition 2020-09-23

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/DIS 18113-4:2021)
Edition 2021-09-01

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2021)
Edition 2021-09-01

Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
Edition 2021-12-01

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)
Edition 2024-08-01