What is an Advertisement?
Legal Framework
Section 44 (1): No person shall advertise a medical device unless the medical device is registered and complies with the Act.
Section 44 (2): Advertisements must not make any misleading or fraudulent claims.
Medical Device (Advertising) Regulations 2019
No person shall advertise a registered medical device without approval from the Authority.
To submit an advertisement application for medical devices, please refer to the following guidelines and resources that clarify the requirements for advertisements that require or do not require approval:

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IMPORTANCE NOTICE: 1. Claims Must Be Accurate and Aligned with Registration All advertising claims must strictly align with the product’s approved registration. Claims must be consistent with the intended use, fully supported by documentation. Any advertisement containing exaggerated, unsupported, or unapproved claims will be rejected. 2. Prohibited Claims and Content All advertisement claims must be developed in accordance with the Code of Advertisement (COA). |
Contact Information
Officers in Charge :
Prepared by: Advertisement Unit ( Pre Market Control Division)
Uploaded by: Corporate Communication Division
Date of upload: 5 February 2026
Notification of Export Only Medical Device
1. Introduction
2. Requirements for Notification of Export Only Medical Device
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No |
Documents
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1 |
Registrar of Companies (ROC) certificate of applicant |
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2 |
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3 |
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4 |
(Please refer to Figure 2: Determination whether LOA is required or not for Export Only Exemption) |
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5 |
A copy manufacturer’s QMS ISO 13485 certificate |
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6 |
A copy of Brochure/Leaflet/Label/IFU that contain information on brief description and intended use. |
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7 |
A copy of establishment license (If applicable) |
Note: *new requirements for Notification of Export Only Medical Device
3. Determination whether LOA is required or not for Notification of Export Only Medical Device?

Figure 1: Determination whether LOA is required or not for Notification of Export Only Medical Device
4. Notification of Export Only Medical Device Process

Figure 2: Notification of Export Only Medical Device Process
5. Fees for Notification of Export Only Medical Device
The payment RM500 shall be made online via portal BayarNow. For guidance on online payment is accessible via link or qr code below:

6. Issuance of Export Only Medical Device Exemption Letter
Any inquiries please email to exportonly.ec@mda.gov.my
General Line: +603 8230 0300
Direct Line : +603 8230 0253 (Pn. Nur Aisyah)
+603 8230 0208 (Pn. Hafizah)
Updated: 25 / 10 / 2023
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No |
Title |
Download |
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1. |
User Manual: i.Establishment Licence Application ii.Renewal of Establishment Licence Application iii. Amendment Major/Minor Application iv. Withdrawal Application |
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2. |
User Manual for Change Of Ownership Application |
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3. |
User Manual Video of Establishment Licence Application |
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4. |
User Manual Video for Renewal of Establishment Licence Application |
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5. |
User Manual Video of Amendment Major/Minor Application |
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6. |
User Manual Video of Withdrawal Application |
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7. |
User Manual Video of Change Of Ownership Application |
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8. |
Guidance Document of Licensing for Establishment |
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9. |
Guidance Document for Good Distribution Practice for Medical Devices (GDPMD) |
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10. |
Guidance Document for Change Of Ownership Application |
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ANNOUNCEMENT ON MDA CONSULTANCY SERVICES
MDA offers regulatory consulting that can support stakeholders who are involve in regulatory submission for medical devices in Malaysia, to comply with medical device regulatory requirements under Medical Device Act 2012 (Act 737). The regulatory consulting services include:
Online consultancy maybe requested for applicant who isn’t physically able to meet MDA’s consultancy team. Consultancy *fee imposed is based on type of consultancy services selected.
*Note: Please refer to Consultancy Request Form (Package) and Consultancy Request Form (Non-Package)
The following diagram describes the step-by-step process of requesting our consultancy services:

If you want to know more about our consultancy services, send an email to consultation@mda.gov.my
Updated: 21 August 2023
Local companies wishing to apply for Certificate of Free Sale (CFS) / Manufacturing Certificate (MC), please CLICK HERE for online application.
ANNOUNCEMENT:
Conditions and fee structure:
Step for Application:
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Documents |
Certificate of free sale |
Manufacturing Certificate (export only manufacturer) |
Manufacturing Certificate (OEM manufacturer) |
|
Registrar of Companies (ROC) certificate of applicant |
Yes |
Yes |
Yes |
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A copy of establishment license |
Yes |
Yes |
Not applicable |
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Proof of medical device registration (Notification letter / Acknowledgement letter/ Registration certificate) |
Yes |
Yes |
Not applicable |
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Yes |
Yes |
Yes |
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Letter of declaration as OEM |
Not applicable |
Not applicable |
Yes |
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Brochure |
No |
No |
Yes |
(And any other additional information, particulars /documents as may be required)
PAYMENT:
Additional information
Additional information, particulars and documents requested by the Authority on the application shall be submitted by the applicant within 14 working days from the date of return of application. If the additional information, particulars or document of the application is not given by the applicant within the time granted (14 working days), the application shall be deemed to be withdrawn and shall not be further proceed with, but without affecting the right of the applicant to make a fresh application.
Complete submission for certificate of free sales application will be processed within 14 working days
The above requirement is subject to change from time to time.
Any enquiries can be sent to Medical Device Authority (MDA) at the following address:
Chief Executive
Medical Device Authority (MDA), Ministry of Health Malaysia
Level 6, Prima 9, Prima Avenue II,
Block 3547, Persiaran APEC, 63000 Cyberjaya,
Selangor, MALAYSIA
Tel: +603-8230 0300 | Fax : +063-8230 0200
Or, please contact:
1) Mr Fezri Aziz +03-8230 0395
Email: cfs@mda.gov.my
2) Mr Fadhli Zil +03-82300357
Email: cfs@mda.gov.my
Updated: 27 October 2025
Prepared by: International & Industry Relations Division
Uploaded by: Corporate Communication Division