1. 28TH GHWP ANNUAL MEETING IN KUALA LUMPUR, MALAYSIA

    

2. INTERNATIONAL MEDICAL DEVICE EXHIBITION CONFERENCE (IMDEC 2024)

    

1. MDA TRAINING CALENDAR YEAR 2025

2. In-Depth Training on General Medical Devices

3. Training of Import and Export of Medical Device Requirements

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.

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