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Medical Device Authority Register (MDAR)
Medical Device Centralised Online Application System 2.0 (MEDCAST 2.0+)
Medical Device Technical Competency Online System (MEDTCOMP)
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+)
Medical Device Technical Competency Online System (MEDTCOMP)
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)

News

PRA PELANCARAN IMDEC 2026: LANGKAH BESAR…

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PUTRAJAYA, 15 OKTOBER 2025 – Pihak Berkuasa Peranti Perubatan (MDA) di bawah Kementerian Kesihatan Malaysia...

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DRB-HICOM ADAKAN KUNJUNGAN RASMI KE MDA …

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    CYBERJAYA, 10 Oktober 2025 – Pihak DRB-HICOM telah mengadakan kunjungan rasmi ke Pejabat Pihak Berkuasa...

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PERTANDINGAN PIDATO PERANTI PERUBATAN SE…

CYBERJAYA, 7 Oktober 2025 – Program Kesedaran Awam Peranti Perubatan 2025 anjuran Pihak Berkuasa Peranti...

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KEMERIAHAN PROGRAM KESEDARAN AWAM PERANT…

CYBERJAYA, 7 Oktober 2025 – Program Kesedaran Awam Peranti Perubatan anjuran Pihak Berkuasa Peranti Perubatan...

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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.

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

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  • Last Updated: 17 October 2025.

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