Project
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific
Begin
2022-12-19
Planned document number
ISO 15223-1 DAM 1
Responsible national committee
NA 176-01-02 AA - Quality management and corresponding general aspects for medical devices
Responsible international committee
ISO/TC 210/WG 3 - Symbols and nomenclature for medical devices
