The Medical Device Branch is entrusted with the responsibility of regulating medical device products placed on the Singapore market. Our objective is to safeguard public health and safety by implementing regulatory controls through a programme of pre-market assessment of devices, manufacturing controls and post-market vigilance. Medical Device Branch carries out a range of assessment and monitoring activities to ensure medical devices available in Singapore are of an acceptable standard under a Voluntary Product Registration scheme since 1 April 2002.
- Regulatory Updates
- Rejected Registration Applications
- Field Safety Corrective Action Reporting
- Adverse Event Reporting
- Seminar Announcement