Under the Medical Device and Pharmaceutical law in Malaysia, all exhibitor must notify the respective Malaysian Authority in order to be permitted to exhibit its nonregistered medical devices and pharmaceutical products.
Have you done yours?
Avoid the stress, running around in circles and wasting money & resources.
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Date : 7 – 9 July 2020
It is important to know the new specific requirements for your products and the timelines available to make sure that your products and your company are ready for “The NEW CE MARKING”.
Date : 7 – 9 July 2020
T T Medical Management Sdn Bhd is an established Authorised Representative (“AR”) company. We are licensed by the Medical Device Authority (“MDA”) which regulates medical devices under the “Medical Device Act 2012” and “Medical Device Regulations 2012”. Under the regulation, all foreign manufacturers must appoint an AR to submit the registration application of their medical devices. For more details of the MDA , please visit Medical Device Authority (MDA) Malaysia.
