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Medical Device Distribution License (IDAK)

About this service

IDAK (Medical Device Distribution License) is a required permit to distribute imported medical devices in Indonesia. Before products can be circulated, a strict evaluation covering safety, quality, and effectiveness is necessary to ensure products meet national standards. By having an IDAK license, companies can ensure their products are legal for distribution and meet consumer trust in Indonesia. If you need support in the IDAK licensing process, Naramedic is ready to help. Our expert team will guide you through every stage, ensuring all requirements are met efficiently and quickly.

What You Get

Complete preparation and review of IDAK documents according to Ministry of Health standards.

Acceleration of the approval process so the official IDAK document can be issued promptly.

Direct regulatory consultation with an expert team, helping you understand each stage of the IDAK application according to Kemenkes provisions.

If you proceed to the CDAKB process after IDAK, you will receive an official e-Report account from the Ministry of Health to facilitate digital reporting of medical device distribution.

Full support in meeting IDAK requirements, from recommendations for PJT (Technical Person in Charge), drafting notarial agreement deeds, to references for technicians and warehouse equipment according to Kemenkes standards.