Monthly Archives: March 2019

Teeth whitening or bleaching has become a popular esthetic dental treatment. In Thailand, various dental clinics and hospitals offer this service.

Consumer teeth whitening products in toothpaste form, and available in supermarkets and drug stores for home use were classified as cosmetics in previous regulations.

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It is less than a month until CMEF Indonesia 2019, a medical equipment and manufacturing exhibition that brings together international medical equipment brands to connect with locally licensed medical equipment distributors, resellers, manufacturers, regulators, and government agencies. 

We are all geared up to meet you! Andaman Medical is pleased to be a Knowledge Partner for CMEF Indonesia 2019 and we look forward to meeting you at our booth in the Consultancy Lounge. Please feel free to meet our consultants for a chat or to answer your questions…they are always more than happy to help!

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The Medical Device Authority (MDA) in Malaysia launched a new database, MeDC@St 2.0, on the 2nd January 2019 to assist authorized representatives, importers, or distributors in registering their medical devices. As of the 21^st December 2018, all draft applications in MeDC@St 1.0  are not able to be submitted using the previous system. 

All applications that were submitted in MeDC@St 1.0 before 21^st December 2018, and were either in “Processing” or “Pending Payment” will continue to undergo evaluation by the Medical Device Authority (MDA) officer until their approval; however, all new applications for medical device registration must be submitted using MeDC@St 2.0.

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In relation to the 2009 Health Regulation no. 36, which was implemented to drive transparent and accountable public service, the Ministry of Health in Indonesia has published guidance on the procedures to import medical devices through the Special Access Scheme (SAS).

In relation to the 2009 Health Regulation no. 36, which was implemented to drive transparent and accountable public service, the Ministry of Health in Indonesia has published guidance on the procedures to import medical devices through the Special Access Scheme (SAS).

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