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Medical Device Registration Information
Introduction: In accordance with Section 5 (1) of the Medical Device Act 2012 (Act 737), no medical device shall be imported, exported or placed in the market unless the medical device is registered under this Act.
Definition of Medical Device: Medical device means any instrument, apparatus, implement, machine, appliance, implant, in vitro reagent or calibrator, software, material or other similar or related article intended by the manufacturer to be used, alone or in combination, for human beings for the purpose of:-
- diagnosis, prevention, monitoring, treatment or alleviation of disease;
- diagnosis, monitoring, treatment, alleviation of or compensation for an injury;
- investigation, replacement or modification, or support of the anatomy or of a physiological process;
- support or sustaining life;
- control of conception;
- disinfection of medical device; or
- providing information for medical or diagnostic purpose by means of in vitro examination of specimens derived from the human body, which does not achieve its primary intended action in or on the human body by pharmacological, immunological or metabolic means, but that may be assisted in its intended function by such means.
1. Related Legislation and Circular Letter
5. Rules of Classification
6. Grouping
7. Conformity Assessment for Medical Device
9. Information on Fee Structure for Medical Device Registration
10. Classification and Registration Technical Committee Meeting
b. 2023 Meeting Decision
iii.List of medical device risk classification
iv. List of products (medical device or non-medical device)
iv. List of products (medical device or non-medical device)
c. 2024 Meeting Decision
i. February 2024
i. February 2024
11. New information and announcement
- Aug 2024
- MDA Approach for New and Re-Registration of Medical Devices With Expired EC Certificates and Self-Declared Class B IVD
- Engagement with IVD Establishments & Survey on In-Vitro Diagnostic Issues
- July 2024 - MeDC@St3.0 Project Development Update - License & Registration Modules
- May 2024 - Establishments are Advised to Submit Medical Device Re-Registration Applications in the MeDC@St2.0+ System One year Prior to Certificate Expiration Date.
- Feb 2024 - Medical Device Re-Registration Application: Implementation of Initial MDA Response Within 14 Working Days
- Oct 2023 - Pelaksanaan Penggunaan Sijil Pendaftaran Peranti Perubatan Elektronik Sepenuhnya Bermula 1 November 2023
- June 2023 - MDA Approach on Expired EC Certificate for New Registration and Re-registration of Medical Device - refer to the updated announcement Aug 2024 - MDA Approach for New and Re-Registration of Medical Devices With Expired EC Certificates and Self-Declared Class B IVD.
- March 2023 - Withdrawal of Medical Device Registration (New and Re-Register) And Change of Notification Application
12. Check status of registration
13. Registration Statistic (Year 2023)
14. Frequently Ask Questions (FAQs) – under revision
15. For any inquiries, kindly contact us for further assistance:
a. Registration Unit email address:
i. General email: registration@mda.gov.my
ii. IVD email: ivd.registration@mda.gov.my
iii. Officers’ email and contact number: BKPP Staff Directory
b. Registration Unit telephone number:
i. Extension line: +603 8230 0376
ii. Puan Aidahwaty Ariffin @ Aidahwaty M.Olaybal, A.M.N. (BKPP Director):
ii. Puan Aidahwaty Ariffin @ Aidahwaty M.Olaybal, A.M.N. (BKPP Director):
- Office Number: +603 8230 0341 or
- HP Number (Whatsapp only) : +6016 333 7031
c. For assistance related to MeDC@St2.0+ system technical issues, kindly submit ticket via MeDC@St2.0+ Helpdesk
Medical Device Registration Unit (MEDRU)
Pre-Market Control Division, MDA
Information is updated on 22 August 2024
Pre-Market Control Division, MDA
Information is updated on 22 August 2024