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Medical Device Product Registration and Approval in Indonesia



Medical devices are regulated by the Ministry of Health (MOH) in Indonesia whose objective is to increase the availability, distribution, and affordability of medical devices. They also help to ensure its safety, efficacy, benefits, and quality. Medical devices are regulated under INDONESIA MOH Decree – 1190/2010.


The application for the marketing license of Medical Device importation is submitted by:


  •          The Medical Devices Distributor (PAK) that is in possession of the license from the company or business representative and also has the power as a sole agent acknowledged by the local representative of the Republic of Indonesia, with the appointment term of minimum 2 years;


  •         The Medical Devices Distributor that is a non-sole agent should also possess the power of attorney so as to register the medical device from the medical device production company or from the responsible company overseas; or


  •         The company that is in possession of the production certificate to carry out the reassembling/repacking of imported products.

As per the regulation, the medical devices are classified as Class I, IIa, IIb and III (similar to the term used in Europe MDD). Class A, B, C and D (similar to ASEAN MDD is also adapted in the application form).

The documentation requirements incorporate the elements of ASEAN Common Submission Dossier Template (CSDT), administrative legalization documents, and also some test reports to be verified. There are specific requirements in the test report that requires the manufacturers to comply with to meet the evaluation requirements for the product approval in Indonesia.  


Example of Approval


Source: MoH

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