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:
- Invitation to Socialization Event on Medical Support Devices for Health Services [pdf]
- Slide Material of Inclusion Medical Support Devices for Health Services in e-Catalogue V6 [pdf]
(both provided in Indonesian; English translation is not available)
Level II Categories | Level III Categories |
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Document Requirements
Refer to slide material page 6:
Type | Required Document |
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Product Specifications | ✓ |
Valid Letter of Notification/Surat Keterangan Informasi Produk/SKP-IP | ✓ |
Guarantee information | ✓ |
After-Sales Service and Spare Parts Availability Letter | ✓ |
Pricing Structure | ✓ |
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.