Indonesia: Medical Support Devices Inclusion in e-Catalogue Version 6

This process applies to medical support devices that have received a Letter of Notification (Surat Keterangan Informasi Produk/SKP-IP) from the Ministry of Health, stating that the product is not classified as a medical device. These products are used in health services in accordance with their intended function.

To view the full list of product categories and supporting details, please refer to the following documents:

(both provided in Indonesian; English translation is not available)

Document Requirements

Refer to slide material page 6:

Transition Information:

E-Catalogue Version 6 has not been fully activated yet. During the transition period, Versions 5 and 6 will operate in parallel, with both the old and new systems running simultaneously.

Implications for Clients:

Clients who wish to list their medical support devices in e-Catalogue Version 6 may proceed by completing all the required attributes, as outlined on page 6 of the slide materials.

For more information or assistance, contact us at sales@andamanmed.com or click the button below.

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