Announcement
MEDICAL DEVICE SEMINAR 2024
23 July 2024
LIST OF MEDICAL DEVICE ADVERTISEMENT APPROVAL
22 July 2024
[email protected] PROJECT DEVELOPMENT TIMELINE
05 July 2024
News
FIELD CORRECTIVE ACTION LISTING FOR JUNE…
The list below contains Medical Device’s Field Corrective Action for the month of June 2024...
Read morePROGRAM PROMOSI KESEDARAN KEPADA PENGGUN…
10 Julai 2024 - Program Promosi Kesedaran Kepada Pengguna Akta Peranti Perubatan 2012 (Akta 737)...
Read moreMESYUARAT DUA HALA ANTARA MDA, MALAYSIA …
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3 Julai 2024, Cyberjaya - Mesyuarat Dua Hala antara MDA, Malaysia dan ‘Ministry of Food...
Read moreMESYUARAT DUA HALA ANTARA MDA, MALAYSIA …
![](/images/WhatsApp_Image_2024-07-04_at_06.30.15.jpeg)
3 Julai 2024, Cyberjaya - Mesyuarat Dua Hala antara MDA, Malaysia dan ‘Health Sciences Authority...
Read moreMESYUARAT GLOBAL HARMONIZATION WORKING P…
![](/images/WhatsApp_Image_2024-06-21_at_17.29.06.jpeg)
12 – 13 Jun 2024 – Mesyuarat 'Global Harmonization Working Party Tehnical Committee (GHWP TC)...
Read morePROGRAM TAKLIMAT KESEDARAN PENGGUNA INTE…
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7 Jun 2024 - Program Taklimat Kesedaran Pengguna Internet telah diadakan bertempat di Bilik Mesyuarat...
Read moreSESI LIBAT URUS BERSAMA JURUTEKNIK PERAN…
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SESI LIBAT URUS BERSAMA JURUTEKNIK PERANTI PERUBATAN INSTITUSI KESIHATAN BUKAN DIBAWAH KKM BERKAITAN PROGRAM KAWALAN...
Read moreTraining for Industries
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.
Covid-19 Recent Information
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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
Satisfaction Survey
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