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Announcement

Covid-19 Recent Information

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Suspension and Cancellation of Establishment Licence and Medical Device Registration

Semua establismen yang menjalankan aktiviti meletakkan peranti perubatan dalam pasaran perlu mempunyai Lesen Establismen dan peranti perubatan tersebut perlu didaftarkan seperti yang termaktub dalam Akta Peranti Perubatan 2012 (Akta 737). Orang awam boleh menyemak status Lesen Establismen dan pendaftaran peranti perubatan melalui carian akses di pautan https://mmdr.mda.gov.my/public/. 

Walau bagaimanapun, terdapat establismen yang telah melanggar Akta 737 dan Peraturan Peranti Perubatan 2012. Read more 

News

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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.

For Listing of Recalls & Listing of Field Safety Notice, please Click Here!

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[FIRST ANNOUNCEMENT] MEDICAL DEVICE SEMINAR BY THE MEDICAL DEVICE AUTHORITY - 19 OCTOBER 2023

ANNOUNCEMENT ON MDA TRAININGS IN 2023

[ OFFICIAL ANNOUNCEMENT] MEDICAL DEVICE SEMINAR BY MEDICAL DEVICE AUTHORITY (MDA)

FIRST ANNOUNCEMENT HANDS-ON WORKSHOP EFFICIENT WAY TO PREPARE FOR MDA DOCUMENTATION SUBMISSIONS - 23rd, 24th, 30th OCTOBER 2023

FIRST ANNOUNCEMENT ON COMPULSORY COMPETENCY MODULE FOR BIOMEDICAL TECHNICAL PERSONNEL (BTP) 31st OCTOBER 2023 & 1st NOVEMBER 2023

 

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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
  +603 - 8230 0300
  +603 - 8230 0200 
 

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  • Last Updated: 27 September 2023.
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