To All Stakeholders, Manufacturers, Importers, Distributors, and Users of Medical Devices

It is hereby informed to all stakeholders, including manufacturers, importers, distributors, healthcare providers, and end-users, about updates related to medical devices within our jurisdiction.

Any instrument, apparatus, appliance, software, material or any other article, whether used single or in combination, including the software necessary for its proper application intended by the manufacturer used in or on human beings for the purpose of Laser procedures, Micro needling, Thread lifting, Cavitation, Electro muscle stimulation, High intensity ultrasound tightening and Fraxel radio frequency technology for skin tightening should be registered under the medical devices.

For further information or clarification on any of the above points, please contact Medical Device Regulatory Division, NMRA.

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(Date: 18 January 2024)

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