Thank you for the information. Will update if I have further queries on the requirements. Do give me some time to review it. Also kindly clarify if there are any change to the label on the physical medical device itself?
In addition to the label change, OSTE would like to know if there are any regulatory action required when OSTE adds a data matrix code to the product (like a CE sign) and also update the IfU with a picture to explain the new code.