ГОСТ Р ИСО 14630—2017
[26] ASTM F2503-05. Standard Practice (or Marking Medical Devices and Other Items (or Sa(ety in the Magnetic
Resonance Environment
Правовые нормы для справки
[27] Directive 2001/83/ЕС of the European Parliament and of the Council of 6 November 2001 on the Community code
relating to medicinal products for human use
[28] European Council Directive 93.‘42;EEC of 14 June 1993 concerning medical devices
[29] U.S. Code of Federal Regulations, section CFR 812.5
14