ISO-18113-1 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements | Document Center, Inc.

ISO-18113-1 › Complete Document History
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements

Complete Current Edition:

2ND EDITION - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements - Oct. 1, 2022

Obsolete Revision Information:

1ST EDITION - Part 1: Terms, definitions and general requirements - Dec. 15, 2009