In Vitro Diagnostic Medical Devices Directive (93/42/EEC)
There is a new publications in the OJEU of standards harmonised under the In Vitro Diagnostic Medical Devices Directive:
17th November 2017 2017/C 389/04 4 standards added
- EN ISO 11137-1:2015
Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013) - EN ISO 13485:2016 and EN ISO 13485:2016/AC:2016
Medical devices – Quality management systems – Requirements for regulatory purposes (ISO 13485:2016) - EN ISO 15223-1:2016
Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements (ISO 15223-1:2016, Corrected version 2017-03)