Announcement
ISO 13485:2016 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES
25 November 2023
POSSIBLE WAYS TO REGISTER IVD ANALYZER
16 November 2023
MEDICAL DEVICE ADVERTISEMENT APPROVAL
02 September 2022
PENGUMUMAN PENTING PERMOHONAN IKLAN PERANTI PERUBATAN 2023
08 November 2023
REGULATORY TRAINING - POST MARKET REQUIREMENTS
27 October 2023
Covid-19 Recent Information
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GANGGUAN SEKSUAL ADALAH SATU KESALAHAN
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STOP SEXUAL HARRASMENT
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PERMOHONAN MELAKUKAN KERJA LUAR
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PEKERJAAN LUAR ATAU KERJA SAMBILAN
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KEWAJIPAN MEMATUHI PERATURAN
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ETIKA BEKERJA DARI RUMAH
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RASUAH
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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
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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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| 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: 29 November 2023.
Ministry of Health Malaysia
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