Medical Device Authority (MDA) wishes to inform all industry players and healthcare providers that an updated guidance document has been issued. The update involves the revision of the requirement related to foreign manufacturers as follows:
4.8e) Foreign manufacturers shall provide the name and address on the label. Contact details i.e: email and/or phone number and/or website address are optional for technical assistance.
All stakeholders are advised to refer to the latest version of the guidance document for detailed information.
To access the guidance document, please CLICK HERE.
For further inquiries, please contact:
Guidance document unit
Policy and Strategic Planning Division (DASAR) MDA.
Prepared by: Policy and Strategic Planning Division (DASAR) MDA.
Uploaded by: Corporate Communication Division
Date of publication: 22 May 2026