(2) Our Authorised agent shall, — (a) act as the official representative for obtaining import licence in India. (b) submit all necessary documents, as defined in the Fourth Schedule, for the import licence of medical device. (3) I shall comply with all the conditions imposed on the import licence and with provisions of the Medical Devices Rules, 2017. (4) I declare that M/s............is carrying on the manufacture of the listed medical device at the manufacturing site specified above. (5) I shall allow the Central Licensing Authority or any person authorized by it in that behalf to enter and inspect or audit the manufacturing premise and to examine the process, procedure and documents in respect of any manufacturing site or to take sample of listed medical device for which the application for import licence has been made. (6) In case of any violation of Drugs and Cosmetics Act, 1940 and the Medical Devices Rules, 2017, the authorised agent shall continue to be responsible even after withdraw of this Power of Attorney for the devices imported in India. (7) I do hereby state and declare that all the photocopies or scanned copies in the application are true copies of the original documents. (8) I do hereby state and declare that all the documents submitted by the undersigned are true and correct. Place: Signature of the manufacturer Date: (Name and Designation) Seal/Stamp