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Medical Device Authority Register (MDAR)
Medical Device Centralised Online Application System 2.0 (MEDCAST 2.0+)
Certificate of Free Sale / Manufacturing Certificate (CFS)
MDA Feedback Management System (FEMES)
Regulatory Information Subscription (RIS)
Medical Device Centralized Reporting System (MEDCREST)
Event Management System of Medical Device Authority (EMS)
Mda's e-Training Management System (e-Training)

e-Services

Medical Device Authority Register (MDAR)
Medical Device Centralised Online Application System 2.0 (MEDCAST 2.0+)
Certificate of Free Sale / Manufacturing Certificate (CFS)
MDA Feedback Management System (FEMES)
Regulatory Information Subscription (RIS)
Medical Device Centralized Reporting System (MEDCREST)
Event Management System of Medical Device Authority (EMS)
Mda's e-Training Management System (e-Training)

Training for Industries

Suspension and Cancellation of Establishment Licence and Medical Device Registration

All establishments placing medical devices in the market must possess an Establishment Licence, and the medical devices must be registered as stipulated under the Medical Device Act 2012 (Act 737). The public may verify the status of an Establishment Licence and the registration of medical devices through the search access provided at the following link:

https://mmdr.mda.gov.my/public/

Safety Information

The following documents are summary of some medical device safety information related to potentially hazardous cases. It only serves as a quick reference and in no way should be considered as exhaustive and up-to-date. Please refer to the source of information and your product supplier for details.

Satisfaction Survey

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Satisfaction Survey

Medical Device Authority (MDA),
Ministry of Health Malaysia,
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC,
63000 Cyberjaya, Selangor, MALAYSIA

+603 - 8230 0300

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