In accordance with the European Medical Device Regulation EU/2017/745 (MDR) in effect since 2021, we as an official partner of HEINE Optotechnik GmbH & Co. KG are required to maintain full records of supplied HEINE diagnostic instruments, including name, composition, serial number, and end user.
In accordance with the European Medical Device Regulation EU/2017/745 (MDR) in effect since 2021, we as an official partner of HEINE Optotechnik GmbH & Co. KG are required to maintain full records of supplied HEINE diagnostic instruments, including name, composition, serial number, and end user.
In accordance with the European Medical Device Regulation EU/2017/745 (MDR) in effect since 2021, we as an official partner of HEINE Optotechnik GmbH & Co. KG are required to maintain full records of supplied HEINE diagnostic instruments, including name, composition, serial number, and end user.
