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KERJASAMA MDA DAN MYNIC BERHAD DALAM PEN…
CYBERJAYA, 5 MAC 2025 – Satu sesi Taklimat Kerjasama Penguatkuasaan Pemantauan Penjualan dan Iklan Peranti...
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Kuala Lumpur, 6 Januari 2025 – Pihak Berkuasa Peranti Perubatan (Medical Device Authority – MDA)...
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CYBERJAYA, 5 Februari 2025 - Pihak Berkuasa Peranti Perubatan (MDA) telah menerima Lawatan Kerja dari...
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Cyberjaya, 17 Januari 2025 - Cawangan Kawalan Amalan Perubatan Swasta (CKAPS) melakukan kunjungan hormat ke...
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CYBERJAYA, 14 JANUARI 2025 - Pihak Berkuasa Peranti Perubatan (MDA) telah menganjurkan Majlis Amanat Ketua...
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CYBERJAYA, 7 JANUARI 2025 - Pihak Berkuasa Peranti Perubatan (MDA), Kementerian Kesihatan Malaysia telah mengadakan...
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Pihak Berkuasa Peranti Perubatan (MDA) di bawah Kementerian Kesihatan Malaysia telah dianugerahkan Team of the...
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Training 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
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