What is Import of medical device for personal use?
As, in Covid-19, In this pandemic people face problems to get treatment in hospital, a lots of people died due to reason of service unavailable in time. By use of this you can save life of many people so, why we wait, you can get help of ELT Consultants to know more. We can help you to get permission and we provide all services related to it.
What are the essential condition for getting permission in FORM MD-21?
The Medical device form part of a personal baggage of passenger and use exclusive for passenger.
The Medical device declared as personal baggage to Custom authority.
The passenger import quantities as specified by Registered Medical Practitioner.
The Medical device imported along with invoice or statement which contain the name and quantity of Medical Device.
How to file Application for import of medical devices for personal use?
An Applicant made an application in FORM MD-20 along with accompanying documents.
An applicant also makes sure that the device is used for bonafide purposes.
After filling an application, the Central Licensing Authority after satisfaction with the information and documents enclosed with the application either grants the permission in FORM MD-21 or rejects the application with reason recorded in writing within a period of seven days from the date of application.
ELT Corporate and Medical Device Registration:
ELT Corporate is renowned for its services in all the fields of scientific licenses starting from Legal Metrology, BIS, Drugs and Cosmetics, Medical Devices, Food Safety, Environment safety to New Technology Patent. ELT Corporate has a team of Advocates, Engineers, M.Pharma, Chartered Accountants, Company secretaries. With such a unique combination of talent under a single roof, it has always been a hassle-free wonderful experience for the big Corporates.
ELT Corporate is one of the best medical device consultant in India and always try to provide the best experience to the clients.
How we can help you with Medical Device Registration?
We help our clients to develop all the documents either it may be Device Master File, Quality Manual or Management Responsibility.
We help our clients to maintain various records mandatory as per MDR 2017.
We even provide expert services on developing Quality assurance labs.
We help our clients to communicate with government portals and ministries for getting the license done.
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