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  2. Overview of Regulatory Medical Device. Usage. Certificate Free Sale / Manufacturing Certificate. Notification for Export Only Medical Device. Export Certificate.

  3. Pre-Market Division & Post-Market and Enforcement Division; Policy, International Affairs and Industry Facilitation (DASAR) Management and Service Unit

  4. Corporate Social Responsibility Initiative by the Malaysian Dental Association Eastern Zone in Collaboration with IMARET. Announcement, News. Jul 23, 2024. Highlights of MDA activities 2023-2024. Announcement, News. Jul 4, 2024. Announcement of Flood Relief to Members of the Malaysian Dental Association (MDA) Jul 2, 2024.

  5. 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).

  6. portal.mda.gov.my › index › doc-listGuidance Document

    These Guidance Document was prepared by the Medical Device Authority (MDA) to help the industry and healthcare professionals in their quest to comply with the Medical Device Act (Act 737) and the regulations under it.

  7. 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.

  8. 3 days ago · This facility is provided to enable any interested parties to search for Registered Medical Device, Registered CAB, Licensed Establishments under Section 5, 10, 15 of Medical Device Act 2012 (Act 737) respectively and Notified Medical Device under Medical Device (Exemption) Order 2016.

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