Indonesia: MOH Notification on Medical Device Product Display in E-Catalogue Version 6

Notification Letter No. BJ.01.03/A.VI/6405/2025 regarding the transition of medical device product display to Electronic Catalogue (E-Catalogue) Version 6.

This action follows Circular Letter No. 2 of 2025 from the Head of the Policy Institute for Procurement of Goods/Services (LKPP), which stipulates that E-Catalogue Version 5 for the health showcase will be deactivated on September 30, 2025.

The full Notification Letter is available in Indonesian: [PDF]

Purpose of the Notification

 The Notification aims to:

  • Transition all existing health product listings from Version 5 to Version 6.
  • Ensure that product details are submitted in accordance with the updated attribute guidelines.
  • Provide clear timelines for submission and compliance within the procurement system.

Implications to Clients

For companies with products already approved in the master product list:

  • Product details must be entered into E-Catalogue Version 6 by September 15, 2025.

For companies whose products have not yet been submitted to the master product list:

  • Submission through the E-Catalogue Version 6 system should be completed as soon as possible.

This ensures continuity of product availability within the national procurement process and compliance with LKPP requirements.

Effectivity Date

The notification took effect on September 3, 2025.

For clarification or assistance with Indonesia-related regulatory matters, please contact us at sales@andamanmed.com or click the button below.

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