Indonesia Medical Device Product Registration

Indonesia Medical Device Registration | Andaman Medical

https://andamanmed.com/regulatory-services/medical-device-registration/indonesia/

In order to register a medical device in Indonesia, a company must first obtain a IDAK (Izin Distribusi Alat Kesehatan) or Medical Device Distribution License (MDDL) otherwise …

Indonesia Medical Device Registration - NA …

https://www.pacificbridgemedical.com/regulatory-services/medical-device/product-registration/indonesia/

To prepare for integrating with the ASEAN medical products regulatory system, Indonesia has introduced a new online medical device registration system and now …

Medical Device Registration in Indonesia

https://asiaactual.com/indonesia/medical-device-registration/

Medical Device registration in Indonesia is a relatively fast and inexpensive process particularly considering the size …

Medical Devices Registration in Indonesia - Emerhub

https://emerhub.com/indonesia/medical-devices-registration-indonesia/

Guide to Product Registration in Indonesia …

https://cekindo.com/blog/product-registration-indonesia/

How to Register a Product via BPOM – Basic Requirements. The basic requirements for registering …

Medical device Registration Process In …

https://credevo.com/articles/2021/06/05/medical-device-registration-process-in-indonesia/

After the initiation of universal health care for their citizens in 2014 by the Indonesian government, the growth of the medical devices market improved and led …

Indonesia Medical Device Registration: How To Go …

https://cekindo.com/blog/medical-product-registration-indonesia/

Administrative Documents: Letter of Authorization (LoA), Free Sales Certificate, Production License of Medical Device issued by Indonesian MoH (local product) / ISO 13485 …

Indonesia MoH registration - Qualtech: …

https://www.qualtechs.com/en-gb/indonesia_registration

The registration of medical device in Indonesia is highly regulated by Medical Device and Household Product Assessment Directorate, which is under the Ministry of …

IVD Device Product Registration in Indonesia - Asia Actual

https://asiaactual.com/indonesia/ivd-product-registration/

IVD device definition and classification in Indonesia closely follow GHTF guidelines and are being harmonized according to the ASEAN Medical Devices Directive (AMDD). Official …

Indonesia Medical Device Product Registration - Elsmar Cove …

https://elsmar.com/elsmarqualityforum/threads/indonesia-medical-device-product-registration.39468/

It seems to be under the MOH now and like you, I can't understand their lingo. Try contacting them using this address or seek help from our local 'MATRADE' or …