- Home
- About Us
- Products & Services
- Our Services
- License Representative
- Product Registration
- Medical Device Company Establishment Service
- Renewal and License Amendment
- Miscellaneous Certificates
- Post-Marketing Surveillance
- E- Catalogue
- Medical Device Trademark Management
- GDPMD (Good Distribution Practice for Medical Device)
- Regulatory Intelligence
- research material products
- Our Services
- Articel
- Asia Regulatory Information
- Our Clients
- Gallery
- Contact US
In accordance to carry out product supervision of Medical Devices and Household Health Supplies (PKRT) with Law Number 17/2023 concerning Health, The Ministry of Health issued Circular Letter Number HK.02.02/E/2379/2023 on December 5th. This circular letter is regarding the list of medical device and PKRT testing laboratory networks that have been accredited with SNI ISO/IEC 17025:2017. The availability of these laboratories aims to support the quality assurance of medical devices and PKRT through pre-market and post-market testing, including domestic products.
List of Accredited Laboratory Network
To ensure that medical devices and PKRT meet the safety, quality, and benefit requirements, it is important to rely on accredited testing laboratories. The list of testing laboratory networks listed in Annex 2 of circular provides complete information on laboratories that have obtained SNI ISO/IEC 17025:2017 accreditation. This accreditation covers the scope of medical device and/or PKRT testing.
Benefits of Laboratory Network
The owner of the product approval / license holder, as one of the relevant stakeholders, can utilize this list of laboratories to ensure that their products have undergone rigorous testing and are in accordance with applicable standards. Pre-market and post-market testing will help ensure the safety and quality of products, including domestic products. This laboratory network is an integral part of efforts to monitor and improve the quality of health products.
Periodic Updating of Information
It is important to note that the list of laboratories as well as information related to products, test types, and test methods will be updated regularly. This update will be carried out in line with the development of strengthening the network of medical device and PKRT testing laboratories. This is done in order to always maintain its relevance and be able to accommodate the latest developments in the health sector.
Source :
Artikel Lainnya
-
Human-Derived Products In Indonesian Medical Device Regulation
-
Complete Guide to CDAKB 2026: Who Is Required to Comply, and What Has Changed
-
How to Set Up a Medical Device PT in Indonesia: Step-by-Step Guide 2026
-
Complete Guide to Medical Device Registration in Indonesia 2026
-
How to Find the Right Medical Device Distributor in Indonesia
Our Services
- License Representative
- Product Registration
- Medical Device Company Establishment Service
- Renewal and License Amendment
- Miscellaneous Certificates
- Post-Marketing Surveillance
- E- Catalogue
- Medical Device Trademark Management
- GDPMD (Good Distribution Practice for Medical Device)
- Regulatory Intelligence
- IDAK (Izin Distributor Alat Kesehatan)