Part 2 Making available on the market and putting into service under Regulation (EU) 2017/745

1. 5Reprocessing of single-use devices
2. 6Requirement on health institutions to provide information relating to implanted devices
3. 7Registration of custom-made devices
4. 8Certificates of free sale - fee
5. 9Retention of documentation relating to conformity assessments and custom-made devices
6. 10UK(NI) indication