Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices. Non-critical medical devices
Edition 2021-02-26

Implants for surgery - Active implantable medical devices - Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
Edition 2014-08

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4 : in vitro diagnostic reagents for self-testing.

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing.

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2 : in vitro diagnostic reagents for professional use (ISO 18113-2:2009).

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3 : in vitro diagnostic instruments for professional use (ISO 18113-3:2009).

Air quality - Assessment of air quality monitoring equipment - Part 2: initial assessment of the manufacturer's quality management system and post certification surveillance for the manufacturing process
Edition 2023-07-05

Radiofrequency identification of animals - Part 1: evaluation of conformance of RFID transponders with ISO 11784 and ISO 11785 (including granting and use of a manufacturer code)
Edition 2017-12-29

Flexible sheets for waterproofing - Statistical definition of manufacturer's limiting value and declared value (MLV and MDV) - 95 % Statistic
Edition 2014-01-08

In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
Edition 2013-08