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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://mdar.mda.gov.my/

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

News

All news

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!

e-Services

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Satisfaction Survey

 Dear our valued customers,

Medical Device Authority (MDA) is constantly trying to enhance the quality of our service to all our customers. To achieve this objective, we would like to request you to give your feedback by completing the survey of Customer Satisfaction Survey Form. MDA will not disclose any of your personal information to any party. This survey will be closed on 31 December 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: 01 December 2023.
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